Relevant bibliographies by topics / Formulation evaluation

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Formulation evaluation'

Author: Grafiati
Published: 7 June 2025
Last updated: 16 July 2025

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Journal articles on the topic "Formulation evaluation"

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Guggila Niharika, Mekala Pallavi, and Arumugam Yasodha. "Formulation and evaluation of Ebastine transferosomes." World Journal of Biology Pharmacy and Health Sciences 19, no. 1 (2024): 393–400. http://dx.doi.org/10.30574/wjbphs.2024.19.1.0446.

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The present study was focused on formulating and evaluating Ebastine containing Transferosomes formulation for in vitro studies. Transferosomes formulations were prepared by using cold method and were evaluated for in vitro characteristics, stability studies. Transferosomes formulation displayed highest entrapment efficiency with desired particle size. SEM analyses showed that Transferosomes formulation was spherical in shape. Transferosomes containing lipid higher percentage of drug release after 8 h as compared to other formulations. F-2 formulation was found to be stable at the end of the study on storage condition. The present study suggested that Transferosomes gel formulations provide sustained and prolonged delivery of drug with enhance bioavailability.
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Guggila, Niharika, Pallavi Mekala, and Yasodha Arumugam. "Formulation and evaluation of Ebastine transferosomes." World Journal of Biology Pharmacy and Health Sciences 19, no. 1 (2024): 393–400. https://doi.org/10.5281/zenodo.13789923.

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The present study was focused on formulating and evaluating Ebastine containing Transferosomes formulation for&nbsp;<em>in vitro</em>&nbsp;studies. Transferosomes formulations were prepared by using cold method and were evaluated for&nbsp;<em>in vitro</em> characteristics, stability studies. Transferosomes formulation displayed highest entrapment efficiency with desired particle size. SEM analyses showed that Transferosomes formulation was spherical in shape. Transferosomes containing lipid higher percentage of drug release after 8 h as compared to other formulations. F-2 formulation was found to be stable at the end of the study on storage condition. The present study suggested that Transferosomes gel formulations provide sustained and prolonged delivery of drug with enhance bioavailability.
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Ashok, Kumar Sharma, Pushpendra Singh Naruka Dr., Shankar Soni Mr., Mohit Khandelwal Mr., Shaneza Aman Ms., and Sharma Mukesh. "DEVELOPMENT AND EVALUATION HYDROGEL OF KETOCONAZOLE." International Journal of Current Pharmaceutical Review and Research 11, no. 3 (2019): 01–11. https://doi.org/10.5281/zenodo.12672946.

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The main aim of this study was to develop a topical drug delivery (Hydrogel) ofKetoconazole to reduce the dose of the active drug, to improve patient compliance, to avoidthe side effects and increase local onset absorption and action. Ketoconazole interfarewith 14-&alpha; sterol demethylase, a cytochrome P-450 enzyme essential for conversion oflanosterol to ergosterol. These turn in inhibition in synthesis of ergosterol and also enhancecellular permeability of fungus due to reduced amounts of ergosterol present in the fungal cellmembrane. Methods: Topical Hydrogel formulations development of Ketoconazole wasprepared by using Different-different polymers by enhancer stability and viscosity with theirdifferent concentrations. Six different formulations of Ketoconazole were prepared andevaluated parameters with respect to their colour, Spreadability, viscosity, determination ofpH, drug content of formulations, in vitro drug release studies, and stability studies. Results:FT-IR study results that there were not any interaction between the drug, Polymers, andexcipients. All the developed formulations of Ketoconazole show acceptable standardphysical properties. The drug content and percentage yield were higher for F5 formulationamong all formulation. F5 shows better drug release. Stability study of the best formulationF5 with guar gum polymer was found with best results. Conclusion: From the aboveobservation results that this F5 formulation may be more effective topical formulation for thehealing of fungal infections in the skin.&nbsp;
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Thakur, R. S., A. Nayaz, and Y. Koushik. "Formulation and Evaluation of Solubility Enhanced Ciprofloxacin." International Journal of Pharmaceutical Sciences and Nanotechnology 6, no. 3 (2013): 2131–36. http://dx.doi.org/10.37285/ijpsn.2013.6.3.4.

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In the case of solubility limited absorption, creating supersaturation in the GI fluid is very critical as supersaturation may provide great improvement of oral absorption. The techniques to create the so-called supersaturation in the GI fluid include microemulsions, emulsions, liposomes, complexations, polymeric micelles, and conventional micelles. Ciprofloxacin was chosen because it is practically insoluble in water; hence its salt form is used commercially, which is soluble in water. The objective of the present investigation was to enhance the solubility of Ciprofloxacin by formulating it into microemulsion system. For this purpose, initially, surfactant and cosurfactant were selected based on their HLB value, followed by pseudo-ternary phase diagrams to identify the microemulsion existing zone. Different formulations were developed and evaluated for pH, conductivity, in vitro release and stability. Solubility study was performed for optimized formulation. The pH of the designed formulations varied from 6.02-7.04. This was ideal and near blood pH 7.4. Conductivity data indicated that the microemulsion was of the o/w type. In vitro release of optimized formulation(FM3) was 95.2% as compared to pure drug 46.61% after 90 min and marketed product(salt form) 93.9%. Hence, by formulating into microemulsion, the solubility of ciprofloxacin is significantly enhanced. &#x0D;
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Gayathri, B. Leela, T. Pavani, P. Ram Prathap, et al. "Formulation and evaluation of dipotassium clorazepate topical gels." International Journal of Experimental and Biomedical Research 4, no. 1 (2025): 26–36. https://doi.org/10.26452/ijebr.v4i1.719.

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This investigation aimed to formulate and evaluate a topical gel containing dipotassium clorazepate. To achieve the desired drug release, a topical gel containing dipotassium clorazepate was synthesized using the dispersion method. Three different gelling agents, carbopol 934p, HPMC K100, and sodium alginate, were used in four different ratios. Twelve gel formulations of dipotassium clorazepate that had been prepared were assessed for stability, drug release kinetics, drug diffusion, pH measurement, viscosity, and drug content. Drug-polymer compatibility studies were done using the Fourier Transform Infra Red (FTIR) spectrophotometer. The absence of extraneous interactions among excipients was established using FTIR. F4 released 98.53% of the drug after the eighth hour and was regarded as the best formulation. Thus, formulations containing Carbopol outperformed other formulations. Even after 6 months, the stability investigation revealed no significant change in the optimum formulation's drug content analysis or in-vitro dissolution study. The stability data were analyzed using the "Stab" software, and the anticipated shelf life term for the best formulation was 12.14 months.
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Saini, Tanishk, Manvi Sharma, Deepti Katiyar, Priya Bansal, and Jagannath Sahoo. "FORMULATION AND EVALUATION OF ANTHELMINTIC HERBAL FORMULATIONS." International Journal of Research in Ayurveda and Pharmacy 9, no. 3 (2018): 205–8. http://dx.doi.org/10.7897/2277-4343.09394.

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Sohel, Shaikh Tejashri Kedar Abubakar Shaikh Aman Shaikh Devang Shah. "Formulation And Evaluation Of Herbal Hair Oil." International Journal of Pharmaceutical Sciences 2, no. 5 (2024): 1851–65. https://doi.org/10.5281/zenodo.11403273.

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Currently, shampoo, conditioners and also some hair tonics formulations using the herbal extract are popular hair care products.&nbsp; The herbal hair oils are critical part of herbal natural cosmetics. The herbal formulations probably have less side effects as compare with the synthetic one. &nbsp;The main goal of present study is the preparation of herbal hair oil using the various herbal ingredients like curry leaves, rose petals, hibiscus, rosemary, meth, coconut oil, almond oil, and also evaluation of herbal oil formulation was performed by determining various parameters, like pH, viscosity, saponification value and are reported in this paper. &nbsp;&nbsp;By taking mixture of above crude drugs the formulation was prepared by the boiling method in the form of hair oil. Herbal hair oil is greater and also used in lot of aliments of hair. &nbsp;From the both prepared formulations F1 formulation have characteristic results.&nbsp; This prepared formulation has anti-hair fall and also other properties such as anti-dandruff effect, reduces hair pigment, helps to improve blood circulation of the scalp and roots, reduces hair graying, anti-fungal effect.
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Khan, Rahman Ullah, Shefaat Ullah Shah, Sheikh Abdur Rashid, et al. "Lornoxicam-Loaded Chitosan-Decorated Nanoemulsion: Preparation and In Vitro Evaluation for Enhanced Transdermal Delivery." Polymers 14, no. 9 (2022): 1922. http://dx.doi.org/10.3390/polym14091922.

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Nanoemulsions are promising drug delivery systems for the administration of poorly soluble drugs like lornoxicam (LRX) by oral or parenteral routes. Such formulations work perfectly for transdermal delivery of lornoxicam-type drugs. It has also been established that formulating such a delivery system is highly dependent on the presence, type, and concentration of excipients taking part in the formulation. The inherent characteristics of nanoemulsion (NE), i.e., smaller globule size and excipient nature, facilitate the drug’s passage through skin. The current study was aimed at the development of an NE-based formulation of LRX to improve the drug solubility in vitro as well as to enhance drug skin permeation to promote therapeutic outcome in appropriate time. Spontaneous self-emulsification technique was utilized to develop optimized LRX-encapsulated NE-based formulations. ATR-FTIR spectra of the pure drug and various formulations did not show any interaction between the drug and various formulation excipients showing compatibility. Globule size for stable formulations ranged between 63–168 nm. These formulations were characterized for viscosity, surface tension, pH, drug encapsulation efficiency, in vitro drug release, and drug skin permeation studies. Chitosan-decorated optimized NE formulation of LRX showed about 58.82% cumulative drug release, showing an anomalous non-Fickian diffusion mechanism of drug release. Drug encapsulation efficiency, in vitro drug release, and skin permeation studies exhibited promising results. An appreciable drug entrapment efficiency was exhibited by optimized NE formulations LRX-6, 71.91 ± 3.17% and C-LRX, 65.25 ± 4.89%. Permeability parameters like enhancement ratio (Er), permeability constant (Kp), and steady state flux (Jss) showed higher values and exhibited good results based on formulation type. The selected promising formulation type “LRX-6” showed significantly different results as compared to other formulations (LRX-4, 5, and 7). The skin permeation property of the LRX-6 formulation was compared to similar chitosan-based formulations and was found to have better skin permeation results than chitosan-based formulations. This study clearly exhibited that an LRX-containing NE-based formulation can be formulated to form a stable drug delivery system. Such formulations are promising in terms of physicochemical characteristics, improved solubility, and high skin permeation potential.
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Srinivasan, Uma Shankar Marakanam, Vishnu Vishnu, Sharmila Sharmila, and Amod Kumar. "FORMULATION AND EVALUATION OF CEFIXIME TRIHYDRATE TOPICAL GEL FOR WOUND INFECTIONS." Asian Journal of Pharmaceutical and Clinical Research 11, no. 8 (2018): 369. http://dx.doi.org/10.22159/ajpcr.2018.v11i8.26150.

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Objective: The objective of this research work was to formulate and evaluate topical gel loaded with cefixime trihydrate, a third-generation cephalosporin antibiotic for the treatment of bacterial wound infections.Methods: The cefixime trihydrate gel was formulated using polymers such as Carbopol 940 and hydroxypropyl methylcellulose E4M in varying concentrations. Three different formulations were prepared and characterized physically for color, syneresis, spreadability, pH, drug content, and rheological properties. In vitro drug release in phosphate buffer pH 7.4 and antibacterial study were performed for the gel formulation to evaluate its therapeutic effect on wound infections.Results: The study demonstrated that the gel formulations showed promising results on their physical evaluation tests. The rheology behavior of the gel was shear-thinning flow type which indicated easy spreading of the gel. The drug release of the gel formulation F2 was selected as the best due to its highest drug release rate of 32.2% in comparison with the other two formulations after 2 h of the study. F2 formulation possessed the highest antibacterial activity as compared to other two formulations.Conclusion: A pioneering work was done on formulating cefixime trihydrate as a gel for topical administration. The antibacterial effect of the drug as gel formulation showed promising effect. We conclude that the cefixime trihydrate could be successively loaded into a gel formulation and can be used for effectively for wound infections like diabetic foot wounds.
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Polishetty, Saipriya* Mariyam Suryaprakash Reddy SK. Irfan Khan Afshan Urooj Dr. Y. Krishna Reddy Dr.K. N. V. Rao Dr. K. Rajeswar Dutt. "FORMULATION, OPTIMIZATION AND EVALUATION OF ESLICARBAZEPINE ACETATE." INDO AMERICAN JOURNAL OF PHARMACEUTICAL SCIENCES 05, no. 03 (2018): 1688–93. https://doi.org/10.5281/zenodo.1209355.

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The present study aims at developing an Eslicarbazepine fast dissolving tablet formulation for the effctive treatment of Epilepsy. To provide the patient with the most convenient mode of administration, FDT&rsquo;s will dissolve quickly. A Eslicarbazepine is absorbed to atleast 90% from the gut, independently of food intake. It is quickly metabolized to esclicarbazepine. So the present work was aimed at formulating fast dissolving tablet for Eslicarbazepine, total 6 formulations were developed by using synthetic superdisintigrants like cross caramellose sodium, Crosspovidone, sodium starch glycolate as superdisintigrants, in a different concentration and prepared by direct compression method and prepared tablets were evaluated for pre-compression and post-compression parameters after conducting pre-formulation studies. All the parameters were within the pharmacopoeial limits and drug disintigrations time was 30sec and wetting time was 38sec and the invitro dissolution showed that the drug release was about 100.62 within 15mins in formulation (F5) containing sodium starch glycolate as superdisintigrant, based on these parameters F5 was selected as best formulation. Key words: Epilepsy, Crosspovidone, Sodium Starch Glycolate, Crosscaramellose Sodium, Direct Compression Method.
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Dissertations / Theses on the topic "Formulation evaluation"

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Norton, E. R., and L. J. Clark. "Mepiquat Formulation Evaluation in southeastern Arizona." College of Agriculture, University of Arizona (Tucson, AZ), 2004. http://hdl.handle.net/10150/198107.

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A series of experiments were conducted in 2003 in the Upper Gila River Valley in Safford, AZ to evaluate several different formulations of the plant growth regulator (PGR) Pix manufactured by BASF. Two experiments were conducted at the Safford Agricultural Center (SAC) while the third was conducted on a grower-cooperator field in the same valley. Experiments conducted at SAC involved evaluating the four formulations of Pix (Pix, Pix Plus, Pix Ultra, and Pentia) in a standard (STD) treatment regime and a low rate multiple (LRM) regime. The untreated control plots in both the LRM and STD experiments produced higher yields than any of the other PGR formulations. Comparing only the PGR formulation treatments the Pentia treatment produced the highest yield in both the STD and LRM experiments. No significant differences were observed in fiber quality for either the LRM or STD experiment. The third experiment conducted on a growercooperator field was a Pentia demonstration experiment. Three treatments including a control, a standard, single Pentia application, and an aggressive split application of Pentia were employed. The highest yield was produced in the most aggressive Pentia treatment. Results from this set of experiments demonstrate the importance of incorporating information from plant monitoring techniques when making decisions about PGR applications.
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Antille, Diogenes Luis. "Formulation, utilisation and evaluation of organomineral fertilisers." Thesis, Cranfield University, 2011. http://dspace.lib.cranfield.ac.uk/handle/1826/6853.

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The water industry recognises significant cost advantages in recycling sewage sludge (biosolids) to agricultural land compared with alternative more expensive disposal options such as incineration or landfill. A recent technique was proposed by United Utilities plc for the production of organomineral fertilisers (OMF) from biosolids granules which adds additional nitrogen to the biosolids’ nutrients to form a balanced NPK fertiliser. The aim of this research was to determine the effects in cereal and grass crops of using organomineral fertilisers (OMF) made from nutrients-enriched biosolids granules and to contribute towards the understanding of nutrient management and dynamics in agricultural systems. The research included soil incubation, glasshouse, lysimeters and field studies which used winter wheat (Triticum aestivum L.) and ryegrass (Lolium perenne L.). A theoretical model was developed for fertiliser particle distribution studies which required the determination of key physical properties of the products. Two OMF formulations have been suggested: OMF10 and OMF15 which have the following NPK compositions: 10:4:4 and 15:4:4 respectively. These were suggested for use in grassland as well as arable cropping. The particle trajectory model showed that the particle size range for OMF10 and OMF15 should be between 1.10 and 5.50 mm and between 1.05 and 5.30 mm in diameter respectively. Cont/d.
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Khan, Muhammad. "Solid dispersions : formulation, characterisation, permeability and genomic evaluation." Thesis, Aston University, 2010. http://publications.aston.ac.uk/10306/.

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Poor water solubility is characterised by low dissolution rate and consequently reduced bioavailability. Formulation of solid dispersion of the drug has attracted considerable interest as a means of improving dissolution process of a range of poorly water soluble drugs. This current study investigates the formulation of solid dispersion for a range of poorly water soluble drugs with varying physicochemical properties including paracetamol, sulphamethoxazole, phenacetin, indomethacin, chloramphenicol, phenylbutazone and succinylsulphathiazole. Solid dispersions were prepared using various drugs to polymer ratios. PEG 8000 was selected as a carrier in the solid dispersions. The study revealed that inclusion of drug within the polymeric matrix, ratio of drug to polymer and physicochemical properties of the drug molecules enhance the dissolution rate. Characterisations of the solid dispersions were performed using DSC, FTIR and SEM. These studies revealed that all seven drugs were present in the amorphous form within the solid dispersions and there was a lack of interaction between the PEG 8000 and drug. Stability studies for solid dispersions showed that all seven drugs studied were unstable at accelerated conditions (40°C±2°C/75%RH±5%RH) whereas, they were found to be stable for 12 months at room conditions. Permeability of indomethacin, phenacetin, phenylbutazone and paracetamol were higher for solid dispersions as compared to drug alone across Caco-2 cell monolayers. From the cell uptake studies it was shown that PEG 8000 enhanced rhodamine123 uptake which suggested that PEG 8000 may increase the permeability of these drugs in solid dispersions. Gene expression profiles analyzing the expression changes in the ABC and solute carrier transporter during permeability studies.ABCA10, ABCB4, ABCC12, SLC12A6, MCT13, SLC22A12 and SLC6A6 gene expression were increased by indomethacin alone whereas solid dispersion of indomethacin resulted in a slight increase in expression. ABCC12 and SAMC gene expression was increased in case of paracetamol alone but slightly increased when exposed to solid dispersion of paracetamol.
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Husman, Stephen H., Randy Wegener, and Frank Meizler. "Pix - Dry Flowable vs. Liquid Formulation Performance Evaluation." College of Agriculture, University of Arizona (Tucson, AZ), 1996. http://hdl.handle.net/10150/210771.

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Cotton crop response was evaluated using the growth regulator FIX in a conventional liquid formulation compared to an equivalent rate of a newly developed dry flowable (DF) formulation. The DF formulation will be available in 1996 in water soluble packets with each 57 gram packet the equivalent of one pint liquid PIX. Both formulations regulated plant height and height:node ratios equally.
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Buys, Johannes Jacobus. "Formulation and evaluation of mebendazole dosage forms / Kobus Buys." Thesis, North-West University, 2003. http://hdl.handle.net/10394/190.

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Parasites in the restricted sense are those members of the animal kingdom which derive their means of well-being from other members of the animal kingdom, at the same time depriving their host of some (sometimes all) of its well-being. Parasitic diseases are much more widespread than many people realise. These diseases affect not only impoverished people in remote countries but they can be important health problems for rich and poor throughout the world. Different parasites infect our domestic animals and cause great losses; they have a great influence on the growing, production and overall resistance against other diseases. The best solution to the problem rests in preventing these infections rather than in wring them. They are never beneficial and we must control them effectively. Mebendazole is a synthetic benzirnidazole with a wide spectrum of anthelmintic activity. Three polymorphic forms of mebendazole, identified A, B and C can be formed through controlled crystallisation procedures. Polymorph C is apparently pharmaceutically favoured. It has been clearly demonstrated that a correlation exist between the polymorphism of the active substance and the bioavailability of the finished product. The characterisation of the active substance was done by means of infrared spectroscopy, DSC and X-ray powder diffraction. The first aim of this study was to formulate a chewable tablet appropriate for the multi-dosage of children during a de-worming program. Chewable tablets present an attractive alternative for children who have not yet learned to wash tablets down with water. The second aim was to formulate a gel for dogs and domestic animals which is more viscous than the products on the market. Dosing an animal with a liquid can be difficult, and a sudden movement of the animal often results in spillage. A drug in a gel form is a convenient means for administration to pets, to reduce spillage. Stability tests were carried out over a test period of three months at 5"C, 25°C + 60% RH and 40°C + 75% RH storage conditions for both dosage forms. All the tests complied with the acceptable criteria except for the loss on drying tests done on the chewable tablets. Therefore silica gel should accompany the tablets to prevent this problem. An HPLC method was developed and validated for the simultaneous determination of the preservative, potassium sorbate and the active substance, mebendazole.<br>Thesis (M.Sc. (Pharm.))--North-West University, Potchefstroom Campus, 2003.
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Jayakumar, Jayanthi. "Evaluation of predictive computational modelling in biologic formulation development." Thesis, Massachusetts Institute of Technology, 2017. http://hdl.handle.net/1721.1/112488.

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Thesis: M.B.A., Massachusetts Institute of Technology, Sloan School of Management, in conjunction with the Leaders for Global Operations Program at MIT, 2017.<br>Thesis: S.M., Massachusetts Institute of Technology, Department of Mechanical Engineering, in conjunction with the Leaders for Global Operations Program at MIT, 2017.<br>Cataloged from PDF version of thesis.<br>Includes bibliographical references (pages 81-87).<br>Computational modelling has completely redefined the experimentation process in many industries, allowing large sets of design concepts to be tested quickly and cheaply very early in the innovation process. Harnessing the power of computational modelling for protein drug formulation has numerous, currently unrealized, benefits. This project aims to be the first step in the development of a high throughput predictive computational model to screen for excipients that would decrease protein aggregation in solution and thus increase its stability and enable clinical effectiveness. Protein drug formulation currently relies heavily on empirical evidence from wet-lab experiments and personal experience. During the biologic drug development process, proteins that target specific disease pathways are identified, developed, isolated, and purified. Scientists then conduct a series of wet-lab experiments to identify the optimal formulation that will allow the protein to be used as a drug therapy. A critical part of formulation development is the identification of inactive ingredients called excipients that perform various important functions including prevention of protein aggregation. Despite their critical role in enabling proteins to be effective therapies, very little is understood about excipient-protein interaction. Furthermore, often a limited set of compounds are tested for their use as excipients since wet-lab experiments are expensive and time consuming. This project accomplishes the following goals: ** Identification of databases of compounds that could be used as excipients in biologic formulation; ** Development of a high throughput method to computationally model a target protein and 247 potential excipients; ** Evaluation of potential relationship between computational output and wet-lab results based onxperimentation with 32 of the 247 excipients; ** Recommendations on next steps that include feedback on types of proteins and excipients to be tested for the validation of the method developed in this project.<br>by Jayanthi Jayakumar.<br>M.B.A.<br>S.M.
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Nicol, Christopher Greig. "The formulation of local housing strategies : a critical evaluation." Thesis, Nottingham Trent University, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.336974.

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This thesis examines the housing market, focusing upon the manner in which housing strategies are formulated by local authorities. The case for housing strategies which examine the needs and demands of all housing tenures has been recognised since 1977. At that time, the introduction of Housing Investment Programme and Strategies attempted to focus local housing policy and production in a strategic manner but since then the strategic policy elements have been continuously eroded. Moreover, since 1977 the housing market has changed considerably. The situation that exists at present is one where speculative housebuilders produce most new housing supply, whilst social housing is now largely provided by housing associations, rather than by local authorities. Now would appear to be an opportune time to reexamine the formulation of housing strategies, with a view to producing a strategy which is more attuned to the needs and demands of the housing market in the 1990s. This study investigates the manner in which the local authority may produce housing strategies which are more structured to the housing production processes of the 1990s. In so doing, it focuses upon three main areas. Firstly, the manner in which the housing market requires an integrated overall approach towards housing provision. In practical terms, this would lead local authorities to attempt to integrate, within an enabling context, the roles of the housing and planning departments. Secondly, as the private sector is responsible for most new housing supply, it is important that it is more closely integrated in policy formulation. This thesis suggests that greater co-ordination between the agency of enablement (local authorities) and the agency of implementation (housebuilders) should ensure that policies are more likely to be realised. The third area examined is the degree to which a local authority can gain a better understanding of local housing markets to ensure that more effective local housing strategies are developed.
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Kangausaru, Shakemore Tinashe. "Formulation development, manufacture and evaluation of hydralazine hydrochloride microspheres." Thesis, Rhodes University, 2017. http://hdl.handle.net/10962/59220.

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Shrestha, Govinda B. "Formulation and analysis of a probabilistic uncertainty evaluation technique." Diss., Virginia Tech, 1990. http://hdl.handle.net/10919/39846.

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Lui, Siu-ying, and 呂少英. "Formulation of a child-focused assessment model for child custody evaluation." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 1996. http://hub.hku.hk/bib/B31978149.

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Books on the topic "Formulation evaluation"

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Mehta, Aasha Kapur, B. Venkatappiah, and R. K. Tiwari. Public policy and administration: Formulation, implementation, and evaluation. Edited by Indian Institute of Public Administration. Indian Institute of Public Administration, 2012.

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author, Vetere Arlene, ed. Working Systemically with Families: Formulation, Intervention and Evaluation. Taylor and Francis, 2018.

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Mercado, Cesar M. Simplified project formulation, development management, financial management, monitoring and evaluation. Development Center for Asia Africa Pacific, 2007.

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Ragnarsson, Gert. Evaluation of tabletting properties in performulation and early formulation work. University Uppsala, Faculty of Pharmacy, 1985.

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National Renewable Energy Laboratory (U.S.), ed. Gearbox reliability collaborative analytic formulation for the evaluation of spline couplings. National Renewable Energy Laboratory, 2013.

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Mercado, Cesar M. Guide to integrated project formulation, management, implementation, monitoring and evaluation, and reporting. Development Center for Asia Africa Pacific, 2008.

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Bernabe, Emma J. Fonacier. Language policy formulation, programming, implementation, and evaluation in Philippine education, 1565-1974. Linguistic Society of the Philippines, 1987.

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Sumarsono, ed. Analysis of the 1987 national Indonesian contraceptive prevalence survey: Implications for program evaluation and policy formulation. National Family Planning Coordinating Board, 1991.

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Dahm, S. Legalisation in Turkish squatter settlements (Gecekondus): evaluation of formulation and implementation of the 1980's building amnesty acts. Oxford Brookes University, 1998.

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(Firm), DanRail Consult, Đường sá̆t Việt Nam, and UNDP Viet Nam, eds. Bridge evaluation project for the railway line Hanoi-Ho Chi Minh City: Project identification and formulation : final report. Vietnam Railways, 1993.

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Book chapters on the topic "Formulation evaluation"

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Newman, K. B., S. T. Buckland, B. J. T. Morgan, et al. "Model Formulation and Evaluation." In Modelling Population Dynamics. Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4939-0977-3_5.

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Ida, Nathan. "Finite element formulation." In Numerical Modeling for Electromagnetic Non-Destructive Evaluation. Springer US, 1995. http://dx.doi.org/10.1007/978-1-4757-0560-7_8.

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Thunhurst, Colin. "Policy Formulation, Planning, and Evaluation." In Public Health Intelligence. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-28326-5_8.

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Ma, Jun, and Zaiyan Gong. "Formulation of Automotive HMI Evaluation Indexes." In Research on Automotive Intelligent Cockpit. Springer Nature Singapore, 2024. http://dx.doi.org/10.1007/978-981-99-9951-4_4.

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Gu, Zhen Yu, Ming Xi Tang, and John Hamilton Frazer. "Formulation of Aesthetic Evaluation & Selection." In Design Computing and Cognition ’04. Springer Netherlands, 2004. http://dx.doi.org/10.1007/978-1-4020-2393-4_18.

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Wesch, Roland. "Specific Studies for Formulation Development." In Drug Discovery and Evaluation: Methods in Clinical Pharmacology. Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-319-56637-5_15-1.

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Wesch, Roland. "Specific Studies for Formulation Development." In Drug Discovery and Evaluation: Methods in Clinical Pharmacology. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-319-68864-0_15.

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Wesch, Roland. "Specific Studies for Formulation Development." In Drug Discovery and Evaluation: Methods in Clinical Pharmacology. Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-540-89891-7_15.

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Wright, Daniel R., Jenny L. Krebel, and Alejandro Perez-Jones. "Evaluation of ILS#1420, Standard Test Method for Evaluating Water Conditioning Agents." In Pesticide Formulation and Delivery Systems: 39th Volume, Innovative Formulation, Application and Adjuvant Technologies for Agriculture. ASTM International, 2019. http://dx.doi.org/10.1520/stp161920180077.

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Volden, H., H. D. Rokkjær, A. Göran, and M. Åkerlind. "The NorFor IT system, ration formulation and optimisation." In NorFor - The Nordic feed evaluation system. Wageningen Academic Publishers, 2011. http://dx.doi.org/10.3920/978-90-8686-718-9_15.

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Conference papers on the topic "Formulation evaluation"

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Klie, Hector, Arturo Klie, Ana Ferrer, and Yolanda De-Abreu. "Towards Automated Development and Evaluation of Optimal Corrosion Inhibitor Products." In CONFERENCE 2023. AMPP, 2023. https://doi.org/10.5006/c2023-18783.

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Abstract In this work, a novel analysis approach using an artificial intelligence (AI) framework that automatically helps identify the drivers of a formulation from lab measurements was showcased. This AI framework builds and optimizes models in the form of physics-based equations from small amounts of measurement data. With this approach, the user can overcome the large data requirements of machine learning while building tailored models that outperform traditional analytical and statistical tools. The effectiveness of this modeling framework in helping scientists reduce uncertainty early in the experiment process was demonstrated. This solution allows a significant reduction in the number of experiments required to achieve an optimal formulation. This was accomplished by generating new, custom models from existing data and well-known equations in electrochemistry. Then, these models were used to predict or hypothesize the performance of unseen formulations by altering their control parameters. This study showed the accuracy of these predictions by calculating its error against unseen measurement data.
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Yu, Taehyung, Soo Yong Lee, Hyunjin Hwang, and Kijung Shin. "Prediction Is NOT Classification: On Formulation and Evaluation of Hyperedge Prediction." In 2024 IEEE International Conference on Data Mining Workshops (ICDMW). IEEE, 2024. https://doi.org/10.1109/icdmw65004.2024.00051.

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Yang, Yutao. "Formulating High Performance Coatings with Novel Adhesion Test Methods." In SSPC 2015 Greencoat. SSPC, 2015. https://doi.org/10.5006/s2015-00065.

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Abstract Adhesion performance is required for every coating system. The adhesion between coatings and substrates is one of the most critical determining factors in the overall success of any coating material. Material design and formulation are key components of high-performance coatings and rely heavily on the accurate measurement and evaluation of adhesion in the coating systems. In the course of our technology advancement, new adhesion test methods have been developed to enhance the formulations of water-based coatings and paints. With these new test methods, we can now understand the adhesion of coatings system from several aspects such as elastic modulus (Young’s Modulus) of a coating film on a substrate, wetting, adhesion energy, and so on. The new methods displayed higher resolution and precision for the evaluation of adhesion in some model water-based coating systems, compared to ASTM methods (D4541, D3359). As a result, we now have the ability to accelerate the process of formulating coatings / paints with higher performance.
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Miller, Albert E., Jeffrey Sarnat, Mohan Pujar, Charles Arvin, Kunigahalli L. Vasanth, and Gautam Banerjee. "Evaluation of Cr(VI) Concentration Effects on Aluminum Alloys in the Presence of Oxoanions." In CORROSION 2000. NACE International, 2000. https://doi.org/10.5006/c2000-00284.

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Abstract A green inhibitor formulation has been developed for treating 2024-T3 and 6061-T6 aluminum alloys. The formulation consists of an oxoanion of the form MO4n- and a catalytic amount of chromium (VI) (10μg/L present as dichromate) that is below the EPA safe limit for drinking water of 100μg/L. This inhibitor formulation has been previously tested as a sealant for anodized aluminum alloys. This combination of anodizing and sealing has shown no evidence of corrosion after over 9 months in a salt fog prohesion test environment. This paper presents the results of tests to determine how the same inhibitor formulation performs on a non-anodized surface and how varying the chromium concentration affects the inhibitor’s ability to provide passive protection for the aluminum alloys. Aluminum alloy coupons (2024-T3 and 6061-T6) treated with the same proprietary oxoanion concentration of the original inhibitor formulation but with varying concentrations of chromium were evaluated using potentiodynamic anodic polarization. The study shows that the aluminum alloys in the presence of the oxoanion by itself displays a pseudo-passive region at low voltages, which is stabilized by the addition of Cr(VI) with concentrations as low as 1 μg/L. The presence of Cr(VI) forms a second unstable pseudo-passive region at a higher potential, which is eliminated at a concentration of Cr(VI) 50 μg/L.
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Topole, Klaus G. "Damage evaluation via flexibility formulation." In Smart Structures and Materials '97, edited by Norris Stubbs. SPIE, 1997. http://dx.doi.org/10.1117/12.274651.

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Borigo, C., F. Yan, Y. Liang, and J. L. Rose. "Ultrasonic guided wave vibration formulation." In REVIEW OF PROGRESS IN QUANTITATIVE NONDESTRUCTIVE EVALUATION: Volume 31. AIP, 2012. http://dx.doi.org/10.1063/1.4716234.

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Galan, J. M. "Lamb wave scattering by defects: A hybrid boundary element-finite element formulation." In QUANTITATIVE NONDESTRUCTIVE EVALUATION. AIP, 2002. http://dx.doi.org/10.1063/1.1472801.

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Lei, Wenqiang, Xiangnan He, Maarten de Rijke, and Tat-Seng Chua. "Conversational Recommendation: Formulation, Methods, and Evaluation." In SIGIR '20: The 43rd International ACM SIGIR conference on research and development in Information Retrieval. ACM, 2020. http://dx.doi.org/10.1145/3397271.3401419.

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Saxena, Minoo, and B. S. Kuchekar. "Cocrystal formulation, characterization, and evaluation study." In 2013 International Conference on Advanced Nanomaterials and Emerging Engineering Technologies (ICANMEET). IEEE, 2013. http://dx.doi.org/10.1109/icanmeet.2013.6609385.

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Orfanogianni, T. "A general formulation for LMP evaluation." In 2012 IEEE Power & Energy Society General Meeting. New Energy Horizons - Opportunities and Challenges. IEEE, 2012. http://dx.doi.org/10.1109/pesgm.2012.6345491.

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Reports on the topic "Formulation evaluation"

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Burke, Thomas G., and A. E. Staubus. Evaluation of LEH/LR16 Artificial Blood Formulation. Defense Technical Information Center, 1992. http://dx.doi.org/10.21236/ada248575.

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Guo, Yi, Jonathan Keller, Robert Errichello, and Chris Halse. Gearbox Reliability Collaborative Analytic Formulation for the Evaluation of Spline Couplings. Office of Scientific and Technical Information (OSTI), 2013. http://dx.doi.org/10.2172/1117059.

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Josephson, G. B., C. C. Chapman, and K. H. Albertsen. Process system evaluation: Consolidated letter reports. Volume 3: Formulation of final products. Office of Scientific and Technical Information (OSTI), 1996. http://dx.doi.org/10.2172/464125.

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Burke, Thomas G. Evaluation of Liposome-Encapsulated Hemoglobin/LR16 Formulation as a Potential Blood Substitute. Defense Technical Information Center, 1991. http://dx.doi.org/10.21236/ada233973.

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Burke, Thomas G. Evaluation of Liposome-Encapsulated Hemoglobin/LR16 Formulation as a Potential Blood Substitute. Defense Technical Information Center, 1990. http://dx.doi.org/10.21236/ada229090.

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Ebert, W. L., and J. L. Jerden. Test plan for formulation and evaluation of grouted waste forms with shine process wastes. Office of Scientific and Technical Information (OSTI), 2015. http://dx.doi.org/10.2172/1344877.

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Shekade, Shubhangi, Satish Shirolkar, and Sanjeevani Deshkar. Formulation and evaluation of castor oil containing self-emulsifying pellets by using design of experiment. Peeref, 2023. http://dx.doi.org/10.54985/peeref.2306p5496957.

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Masset, Edoardo, and Howard White. To boldly go where no evaluation has gone before: The CEDIL Evaluation Agenda. Centre for Excellence and Development Impact and Learning (CEDIL), 2019. http://dx.doi.org/10.51744/ceap.

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This paper introduces the rationale behind the establishment of the Centre of Excellence in Development, Impact and Learning (CEDIL) and the challenges it will address. CEDIL was established with funding from the UK Government through the Department for International Development (DFID), with the aim of developing and supporting new methods and approaches in the evaluation of international development interventions in neglected geographic, and thematic areas. CEDIL has concluded its inception phase, which explored new evaluation methods and approaches with a series of papers, workshops, and consultations. This paper sets out CEDIL’s research agenda for the next three years. CEDIL will promote studies in three key areas: 1) unpacking complex interventions with mixed methods approaches, and exploration of mechanisms, 2) generalising evidence through the formulation of mid-level theories of neglected interventions, and 3) promoting evidence use through stakeholder engagement and demonstrating what works within such communication.
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Gerstl, Zev, Thomas L. Potter, David Bosch, et al. Novel Herbicide Formulations for Conservation-Tillage. United States Department of Agriculture, 2009. http://dx.doi.org/10.32747/2009.7591736.bard.

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The overall objective of this study was to develop, optimize and evaluate novel formulations, which reduce herbicide leaching and enhance agronomic efficacy. Numerous studies have demonstrated that CsT promotes environmental quality and enhances sustainable crop production, yet continued use of CsT-practices appears threatened unless cost effective alternative weed control practices can be found. The problem is pressing in the southern portion of the Atlantic Coastal Plain region of the eastern USA where cotton and peanut are produced extensively. This research addressed needs of the region’s farmers for more effective weed control practices for CsT systems. HUJI: CRFs for sulfentrazone and metolachlor were developed and tested based on their solubilizion in cationic micelles and adsorption of the mixed micelles on montmorillonite. A better understanding of solubilizing anionic and nonionic organic molecules in cationic micelles was reached. Both CRFs demonstrated controlled release compared to the commercial formulations. A bioassay in soil columns determined that the new sulfentrazone and metolachlor CRFs significantly improve weed control and reduced leaching (for the latter) in comparison with the commercial formulations. ARO: Two types of CRFs were developed: polymer-clay beads and powdered formulations. Sand filter experiments were conducted to determine the release of the herbicide from the CRFs. The concentration of metolachlor in the initial fractions of the effluent from the commercial formulation reached rather high values, whereas from the alginate-clay formulations and some of the powdered formulations, metolachlor concentrations were low and fairly constant. The movement of metolachlor through a sandy soil from commercial and alginate-clay formulations showed that the CRFs developed significantly reduced the leaching of metolachlor in comparison to the commercial formulation. Mini-flume and simulated rainfall studies indicated that all the CRFs tested increased runoff losses and decreased the amount of metolachlor found in the leachate. ARS: Field and laboratory investigations were conducted on the environmental fate and weed control efficacy of a commercially available, and two CRFs (organo-clay and alginate-encapsulated) of the soil-residual herbicide metolachlor. The environmental fate characteristics and weed control efficacy of these products were compared in rainfall simulations, soil dissipations, greenhouse efficacy trials, and a leaching study. Comparisons were made on the basis of tillage, CsT, and conventional, i.e no surface crop residue at planting (CT). Strip-tillage (ST), a commonly used form of CsT, was practiced. The organo-clay and commercial metolachlor formulations behaved similarly in terms of wash off, runoff, soil dissipation and weed control efficacy. No advantage of the organo-clay over the commercial metolachlor was observed. Alginate encapsulated metolachlor was more promising. The dissipation rate for metolachlor when applied in the alginate formulation was 10 times slower than when the commercial product was used inferring that its use may enhance weed management in cotton and peanut fields in the region. In addition, comparison of alginate and commercial formulations showed that ST can effectively reduce the runoff threat that is commonly associated with granular herbicide application. Studies also showed that use of the alginate CRF has the potential to reduce metolachlor leaching. Overall study findings have indicated that use of granular herbicide formulations may have substantial benefit for ST-system weed management for cotton and peanut production under Atlantic Coastal Plain conditions in the southeastern USA. Commercial development and evaluation at the farm scale appears warranted. Products will likely enhance and maintain CsT use in this and other regions by improving weed control options.
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Bernard, J. A. Formulation and experimental evaluation of closed-form control laws for the rapid maneuvering of reactor neutronic power. Office of Scientific and Technical Information (OSTI), 1989. http://dx.doi.org/10.2172/6841357.

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