Log in

Relevant bibliographies by topics / Evaluation of formulation / Journal articles

To see the other types of publications on this topic, follow the link: Evaluation of formulation.

Journal articles on the topic 'Evaluation of formulation'

Author: Grafiati

Published: 2 June 2025

Last updated: 31 July 2025

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the top 50 journal articles for your research on the topic 'Evaluation of formulation.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Browse journal articles on a wide variety of disciplines and organise your bibliography correctly.

1

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.

Full text

Abstract:

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 s

APA, Harvard, Vancouver, ISO, and other styles

2

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.

Full text

Abstract:

The present study was focused on formulating and evaluating Ebastine containing Transferosomes formulation for <em>in vitro</em> studies. Transferosomes formulations were prepared by using cold method and were evaluated for <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

APA, Harvard, Vancouver, ISO, and other styles

3

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.

Full text

Abstract:

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-α 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 K

APA, Harvard, Vancouver, ISO, and other styles

4

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.

Full text

Abstract:

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

APA, Harvard, Vancouver, ISO, and other styles

5

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.

Full text

Abstract:

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 Tra

APA, Harvard, Vancouver, ISO, and other styles

6

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.

Full text

APA, Harvard, Vancouver, ISO, and other styles

7

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.

Full text

Abstract:

Currently, shampoo, conditioners and also some hair tonics formulations using the herbal extract are popular hair care products.  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.  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, viscosi

APA, Harvard, Vancouver, ISO, and other styles

8

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.

Full text

Abstract:

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

APA, Harvard, Vancouver, ISO, and other styles

9

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.

Full text

Abstract:

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

APA, Harvard, Vancouver, ISO, and other styles

10

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.

Full text

Abstract:

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’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 gly

APA, Harvard, Vancouver, ISO, and other styles

11

Nayak, Sachin, Kirankumar GD, Vikesh ., Pradyumna B, and Sandeshraj . "FORMULATION AND EVALUATION OF HERBAL TOOTHPASTE." Journal of Biological & Scientific Opinion 12, no. 5 (2024): 54–59. http://dx.doi.org/10.7897/2321-6328.12598.

Full text

Abstract:

The present study is concerned with the formulation and evaluation of herbal toothpaste, which contains various properties like tooth abrasives, tooth whitening, anti-caring, antibacterial, anti-inflammatory, desensitivity, etc. The herbal toothpaste was prepared using mango leaf extract and guava leaf extract as active ingredients, along with various excipients, which include calcium carbonate, sodium chloride, sodium lauryl sulphate, sodium benzoate, glycerine, camphor, honey and distilled water. The toothpaste was prepared by homogeneous mixing of all the excipients and the herbal extract.

APA, Harvard, Vancouver, ISO, and other styles

12

Nakka, Samantha A. Jayasree Praneetha. D. *. "FORMULATION AND EVALUATION OF ORODISPERSIBLE TABLETS OF METOCLOPRAMIDE HYDROCHLORIDE." Journal of Scientific Research in Pharmacy 09, no. 08 (2020): 13–18. https://doi.org/10.5281/zenodo.7626012.

Full text

Abstract:

<strong><em>ABSTRACT</em></strong> <strong> Recent advances in novel drug delivery aims to enhance the safety and efficacy of drug molecule by formulating a convenient dosage form for ease of administration and to achieve better patient compliance. One such approach is oral disintegrating tablets. Oro-dispersible tablets are a suitable means of drug delivery system for better patient compliance, rapid onset of action, increased bioavailability. The purpose of the present research was to formulate and evaluate the mouth disintegrating tablets of metoclopramide hydrochloride. Metoclopramide

APA, Harvard, Vancouver, ISO, and other styles

13

Jangid, Vikash, Arindam Chatterjee, Saurabh Pandey, Vikash Agarwal, and Deeksha Sharma. "Formulation and Evaluation of Bi-Layer Tablet of Nebivolol and Nateglinide." Journal of Biomedical and Pharmaceutical Research 12, no. 3 (2023): 34–42. http://dx.doi.org/10.32553/jbpr.v12i3.993.

Full text

Abstract:

In the present work, the Bilayered matrix type tablet were prepared by direct and wet granulation technique, in which immediate release layer ( by direct compression) contains Nebivolol and extended release layer (by wet granulation) contains Nateglinide. All the developed bilayer tablets were evaluated for weight variation, friability, thickness and hardness. The percent deviation from the average weight, friability, thickness and hardness was found to be within the prescribed official limits. Release profile of Nebivolol from formulations indicate that lower MCC (Formulations CF1 and CF3) an

APA, Harvard, Vancouver, ISO, and other styles

14

Venkateswara Reddy, B., and K. Navaneetha. "FORMULATION AND EVALUATION OF SUSTAIN RELEASE CYCLOBENZAPRINE HYDROCHLORIDE PELLETS." INDIAN DRUGS 54, no. 05 (2017): 19–25. http://dx.doi.org/10.53879/id.54.05.10262.

Full text

Abstract:

Cyclobenzaprine Hydrochloride is a centrally acting muscle relaxant which is mostly available in the form of tablets and capsules. The present aim of the study was to develop a sustained release formulation of cyclobenzaprine Hydrochloride pellets using powder layering technique. Nine different formulations of pellets were prepared by using different concentrations of Ethyl Cellulose-50, Hypromellose (HPMC), and PEG 6000 of all formulations, F8 formulation was the optimized formulation. The kinetic studies of F8 formulation was best fitted in the First order model as it had the highest value (

APA, Harvard, Vancouver, ISO, and other styles

15

Priya, B. Panchal G. N. Dhembre* U. T. Jadhao S. T. Thoke D. A. Rathod S. A. Wathore V. R. Kauthekar. "Development And Evaluation Of Orodispersible Film Of Telmisartan." International Journal in Pharmaceutical Sciences 2, no. 10 (2024): 1652–61. https://doi.org/10.5281/zenodo.14000663.

Full text

Abstract:

The objective of this research work was the Development and evaluation of Orodispersible film of Telmisartan as model drug. This formulation was aimed to deliver the quick onset of action of drug Telmisartan in the management of hypertension, so as to enhance patient’s compliance. The orodispersible film of Telmisartan was prepared by solvent casting method. Orodispersible film of Telmisartan was formulated using two different film forming agent HPMC E5 and Pullulan along with crosspovidone as a superdisintegrant.Total six formulations were developed using varying concentration of film f

APA, Harvard, Vancouver, ISO, and other styles

16

YAVUZ, Akif, and Osman Taha SEN. "Novel approaches to assessing brake squeal propensity: comparative evaluation of two index formulations." INTER-NOISE and NOISE-CON Congress and Conference Proceedings 270, no. 4 (2024): 7362–69. http://dx.doi.org/10.3397/in_2024_3952.

Full text

Abstract:

The persistence of brake squeal as a significant NVH issue within automotive brake systems necessitates the development of robust methods for assessing squeal propensity. This study introduces two novel squeal index formulations for assessment purposes and evaluates their performance against the formulation defined by the SAE J2521 standard. Experimental data essential for formulating the squeal index are collected on a controlled mass-sliding belt experiment. Experiments are performed at three different spring stiffness levels, and squeal index formulations are derived based on time and frequ

APA, Harvard, Vancouver, ISO, and other styles

17

., Manishaanjane, Shikha Agrawal, and Amreen Khan. "FORMULATION AND EVALUATION OF NANOSUSPENSION OF VALSARTAN." International Journal of Current Pharmaceutical Research 10, no. 2 (2018): 68. http://dx.doi.org/10.22159/ijcpr.2018v10i2.25874.

Full text

Abstract:

Objective: The objective of the present research work was to formulate and evaluate Valsartan nanosuspension by nanoprecipitation ultra sonication method using different polymers to enhance solubility and bioavailability of the poorly water-soluble drug.Methods: Formulation of nanosuspension of valsartan by nanoprecipitation technique was used. The nanosuspension formulations were prepared using different polymers such as hydroxyl propyl methyl cellulose E50, polyvinyl pyrollidone k-30, polyethene glycol 6000 and sodium lauryl sulphate was used as the surfactant.Results: The formulation of nan

APA, Harvard, Vancouver, ISO, and other styles

18

Yassin, Ghada. "Formulation and Evaluation of Optimized Clotrimazole Emulgel Formulations." British Journal of Pharmaceutical Research 4, no. 9 (2014): 1014–30. http://dx.doi.org/10.9734/bjpr/2014/8495.

Full text

APA, Harvard, Vancouver, ISO, and other styles

19

Maddela, Sudhir, R. R. Manjula, B. Pamula Reddy, et al. "Formulation and Evaluation of Piroxicam Liquid Fill Formulations." Current Trends in Biotechnology and Pharmacy 18, no. 2 (2024): 1705–12. http://dx.doi.org/10.5530/ctbp.2024.2.19.

Full text

APA, Harvard, Vancouver, ISO, and other styles

20

Katta, Ashwini1 K. Kishore and Dr. Gampa Vijay Kumar. "DESIGN, CHARACTERIZATION AND IN VITRO EVALUATION OF RIFAXIMIN EFFERVESCENT FLOATING TABLETS." INDO AMERICAN JOURNAL OF PHARMACEUTICAL SCIENCES 05, no. 12 (2018): 16583–90. https://doi.org/10.5281/zenodo.2429621.

Full text

Abstract:

<em>In the present research work effervescent floating formulation of Rifaximin by using various polymers. Initially analytical method development was done for the drug molecule. Absorption maxima was determined based on that calibration curve was developed by using different concentrations. Gas generating agent sodium bicarbonate was used. Then the formulation was developed by using different concentrations of polymers of various polymers. The formulation blend was subjected to various preformualation studies, flow properties and all the formulations were found to be good indicating that the

APA, Harvard, Vancouver, ISO, and other styles

21

Shivani, Patil* Sanika Patil Varda Joshi. "Formulation And Evaluation of Hydrogel." International Journal of Pharmaceutical Sciences 3, no. 5 (2025): 2494–99. https://doi.org/10.5281/zenodo.15426097.

Full text

Abstract:

The present study deals with the development and characterization of Aloe Vera hydrogel preparation using the inner part of aloe vera leaf, carbapol 934, polyethylene glycol 400, triethanolamine, glycerin, methylparaben, orange oil, distilled water aloe vera pulp is converted into a liquid using the mixer and hydrogel is prepared by a simple dissolving method of other ingredients in a specific manner. Nine formulations were developed which differ in the ratio of hydrogel-forming polymer. All formulations were evaluated for physical evaluation, pH, Spreadability, % moisture content, antibacteri

APA, Harvard, Vancouver, ISO, and other styles

22

Sharma, Ashish, and Dilip Agarwal. "Formulation and Evaluation of Montelukast Sodium Oral Dissolving Film." Asian Journal of Pharmaceutical Research and Development 9, no. 1 (2021): 130–40. http://dx.doi.org/10.22270/ajprd.v9i1.893.

Full text

Abstract:

The preliminary batches were planned for the formulation and development of placebos of fast dissolving film by using solvent casting method. Total 10 formulations were prepared by using concentration of polymer i.e pullulan in different proportion. In formulations F5 to F6 various concentration of pullulan were incorporated as well as in other formulation trails taken with different concentration of different natural i.e Sodium alginate, SSG and synthetic i.e HPMC, eudragit to find out best suitable polymer for the film formation. Among all formulations, formulation F5 was found to be satisfa

APA, Harvard, Vancouver, ISO, and other styles

23

Joshna Booravilli, Janaki Devi Sirisolla, and Shivani Saluru. "Formulation and Evaluation of Ketoconazole Microsponge Topical Gel." International Journal of Research in Pharmaceutical Sciences 13, no. 4 (2022): 382–91. http://dx.doi.org/10.26452/ijrps.v13i4.3630.

Full text

Abstract:

Microsponges are those drug delivery systems which are intended in a way to deliver a minimum dose of the drug or pharmaceutically active ingredient to increase the stability of formulation, to alter drug release profile. Ketoconazole is an imidazole anti-fungal agent belonging to BCS class II. The main objective of this research work is to formulate and evaluate ketoconazole microsponge for topical delivery by using various polymers such eudragit S-100, eudragit L-100 in four ratios 1:2, 1:3, 1:4, 1:5 by quasi emulsion method. The formulations prepared were labelled based on the ratios as ES

APA, Harvard, Vancouver, ISO, and other styles

24

V., Rajalakshmi S., and Vinaya O. G. "FORMULATION DEVELOPMENT, EVALUATION AND OPTIMIZATION OF MEDICATED LIP ROUGE CONTAINING NIOSOMAL ACYCLOVIR FOR THE MANAGEMENT OF RECURRENT HERPES LABIALIS." International Journal of Applied Pharmaceutics 9, no. 6 (2017): 21. http://dx.doi.org/10.22159/ijap.2017v9i6.19349.

Full text

Abstract:

Objective: Aim of the study was to formulate, evaluate and optimize medicated Lip rouge containing acyclovir encapsulated inside a novel vesicular carrier, niosome so that the formulation can improve its membrane penetration. Formulating as a cosmetic Lip rouge formulation will also improve patient compliance in the treatment of herpes labialis.Methods: Acyclovir niosomes were prepared by thin film hydration method. Niosomes were evaluated and were optimized by considering the entrapment efficiency and in vitro release profile. The optimized niosomes were incorporated into lipstick, lip balm a

APA, Harvard, Vancouver, ISO, and other styles

25

Prakash, Gnana. "Formulation and Evaluation of Prolonged-Release Tablets Containing Solid Dispersions of Rosuvastatin Calcium." Future Journal of Pharmaceuticals and Health Sciences 1, no. 4 (2021): 180–85. http://dx.doi.org/10.26452/fjphs.v1i4.180.

Full text

Abstract:

Pharmaceutical Industry is striving hard to improve the dissolution of drugs with limited water solubility. One of the approaches to improve the dissolution rate of poorly soluble drugs is solid dispersion. Hence in the present research, an attempt was made to improve the bioavailability of Rosuvastatin by formulating it as a solid dispersion. The release of Rosuvastatin calcium solid dispersion was prolonged using HPMC. Eudragit L-100 and PEG-6000 were used as carriers. Nine formulations of prolonged-release Rosuvastatin calcium (RS-SD 1 to RS-SD 9) were prepared and evaluated for pre and pos

APA, Harvard, Vancouver, ISO, and other styles

26

Mishra, Anjali. "Formulation and Evaluation of Polyherbal Soap." International Journal of Science and Research (IJSR) 13, no. 11 (2024): 1288–90. http://dx.doi.org/10.21275/sr241120133600.

Full text

APA, Harvard, Vancouver, ISO, and other styles

27

Alta, B. P., Mrs Shireesha, Gattu Haripriya, et al. "Formulation and Evaluation of Herbal Mouthwash." International Journal of Research Publication and Reviews 5, no. 4 (2024): 1421–26. http://dx.doi.org/10.55248/gengpi.5.0424.1119.

Full text

APA, Harvard, Vancouver, ISO, and other styles

28

V., Vane Vaishnavi, Prof Patil N., and Dr Megha T. Salve. "Formulation And Evaluation Of Ornidazole Topical." International Journal of Research Publication and Reviews 6, no. 5 (2025): 13499–503. https://doi.org/10.55248/gengpi.6.0525.1927.

Full text

APA, Harvard, Vancouver, ISO, and other styles

29

Yan, Xin, Qi Zhang, Tao Wang, Yu Luo, and Xianyi Sha. "Evaluation of Different Polysaccharide–Iron Complex Preparations In Vitro and In Vivo." Pharmaceutics 17, no. 3 (2025): 292. https://doi.org/10.3390/pharmaceutics17030292.

Full text

Abstract:

Objectives: Iron-deficiency anemia is one of the most common nutritional deficiencies worldwide. Polysaccharide–iron complexes (PICs), as novel organic iron supplements, have garnered increasing attention due to their high bioavailability, minimal gastrointestinal irritation, and favorable tolerability. However, different formulations of PICs can show significant variations in their physicochemical properties and bioavailability. These factors are crucial for clinical efficacy and safety. Methods: This study selected two formulations of polysaccharide–iron complexes: Formulation A (PIC-coated

APA, Harvard, Vancouver, ISO, and other styles

30

V., Anitha1* L. Gopi2 R. Aishwarya3 L. Akash4 A. Afroze5 A. Abdullah6. "Optimizing Herbal Lozenges: Formulation Techniques and Efficacy Evaluation." International Journal of Pharmaceutical Sciences 2, no. 11 (2024): 59–70. https://doi.org/10.5281/zenodo.14028700.

Full text

Abstract:

This study presents the formulation of herbal lozenges using a heating and congealing technique. A thorough literature review informed the selection of excipients, which included Agar, Acacia, peppermint oil, citric acid, glycerin, PEG 1000, and PEG 8000. The lozenges were evaluated for weight variation, hardness, thickness, friability, disintegration time, and drug content, with all parameters meeting standard limits. Among the formulations, F6 demonstrated the highest drug content at 99.35%. The study concluded that the herbal lozenges, particularly those incorporating agar and acacia, are a

APA, Harvard, Vancouver, ISO, and other styles

31

Kumar, Akepati Sravan, B. Jagadeesh Babu, B. Nageswara Naik, and M. Pradeep Kumar. "Formulation and evaluation of miconazole-loaded nanosponges for topical delivery." International Journal of Experimental and Biomedical Research 4, no. 1 (2025): 16–25. https://doi.org/10.26452/ijebr.v4i1.701.

Full text

Abstract:

In this work, nanosponges were made by solvent evaporation and mixed with miconazole to form a gel. Utilizing the solvent evaporation method, the formulations for the Nanosponges were created with PVA functioning as a co-polymer and rate-retarders HP-? Cyclodextrin and HPMC K4M. FTIR (Fourier Transform Infra-Red) spectroscopy was employed to ascertain the drug's compatibility with those in the formulation. We examined the surface form, yield of manufacture, and efficacy of drug entrapment in nanosponges. The Nanosponges' shape and surface morphology were investigated using scanning electron mi

APA, Harvard, Vancouver, ISO, and other styles

32

Manish Kumar Gupta, Sujit Nagare, Birendra Shrivastava, Supriya Hyam, and Ketaki Dhane. "Development and Evaluation of Topical Polyherbal Formulations for their Antimicrobial Potential." International Journal of Research in Pharmaceutical Sciences 11, no. 4 (2020): 8187–93. http://dx.doi.org/10.26452/ijrps.v11i4.1812.

Full text

Abstract:

The different types of skin diseases caused due to microorganisms. In recent years the use of the traditional medicinal system was increased because of more minor side effects and cost effective. The single herbal drugs were found to be less potent, which can be improved by utilizing more than one herb in the single formulation, known as polyherbal formulation. The present work involved the development and evaluation of the different polyherbal formulations (cream, gel, and emulgel) using natural ingredients. The aim of the present work is to produce a formulation with improved antimicrobial p

APA, Harvard, Vancouver, ISO, and other styles

33

Rajesh, Akki* M.Gayatri Ramya M.Hymavathi P.Dinesh Kumar. "DEVELOPMENT, EVALUATION AND STABILITY OF ZOLEDRONIC ACID I.V INJECTION BY LYOPHILIZATION TECHNIQUE." Indo American Journal of Pharmaceutical Sciences 04, no. 07 (2017): 2042–46. https://doi.org/10.5281/zenodo.834723.

Full text

Abstract:

The objective of the study is to develop a stable lyophilized formulation of Zoledronic acid for injection for better stability and for long term storage. The lyophilized product of all the formulations (F1- F6) prepared were an appearance of white to white Lyophilized cake. mannitol was used with water for injection . The filled vials were loaded into lyophilizer and lyophilized them as per cycle. Different composition of additives was used and the different pH concentrations of 5.7 to 6.7 were adjusted with sodium citrate were tried to formulate the formulation. The pH of all the formulation

APA, Harvard, Vancouver, ISO, and other styles

34

Hiwse, Ravindra, Rajat Pawar, and Sunita Patidar. "Formulation and Evaluation of Fast Dissolving Film of Imipramine Hcl." International Journal of Pharmaceutical Sciences and Medicine 7, no. 1 (2022): 59–80. http://dx.doi.org/10.47760/ijpsm.2022.v07i01.003.

Full text

Abstract:

This research work was aimed to provide faster onset of action of Imipramine Hcl (used for the treatment depression and bed wetting) by formulating its fast-dissolving film (FDF). Imipramine Hcl belongs to BCS I. The FDF of Imipramine Hcl was prepared by solvent casting method using HPMC (film forming agent), Glycerol (plasticizer), Citric acid (saliva stimulating agent), Mannitol (sweetening agent). The formulation was optimized by two factors, three levels (32) was used for the formulation optimization of fast dissolving film of Imipramine Hcl and experimental trials are performed on all 9 f

APA, Harvard, Vancouver, ISO, and other styles

35

Mayur, Dukare* Rafey Shaikh Rutuja Hirde Gaurav Sonune Surbhi Rawka Dr. Rao Javvaji. "Formulation and Evaluation of Herbal Shampoo." International Journal of Pharmaceutical Sciences 3, no. 6 (2025): 137–43. https://doi.org/10.5281/zenodo.15572106.

Full text

Abstract:

The increasing demand for natural and eco-friendly cosmetic products has led to the development of herbal shampoos as alternatives to synthetic formulations. This study focuses on the formulation and evaluation of a herbal shampoo using various plant-based ingredients known for their cleansing, conditioning, and antimicrobial properties. Selected herbs such as Neem, Acacia concinna (Shikakai), Hibiscus rosa-sinensis, Aloe vera, and Phyllanthus emblica (Amla) were used in the formulation. The prepared shampoo was evaluated for physicochemical parameters including pH, viscosity, foam stability,

APA, Harvard, Vancouver, ISO, and other styles

36

Pandey, Prateek, Anil Sharma, Hariom Sharma, Girish Kumar Vyas, and Manmohan Sharma. "Novel Researched Herbal Sunscreen Cream SPF Determination by In-Vitro Model." Asian Journal of Pharmaceutical Research and Development 11, no. 2 (2023): 83–90. http://dx.doi.org/10.22270/ajprd.v11i2.1246.

Full text

Abstract:

INTRODUCTION: Researchers' interest in creating novel cosmetic formulations has increased due to consumer interest in herbal cosmetics and increased patent activity. The rights of indigenous traditional knowledge and benefit sharing are also safeguarded under IPR. OBJECTIVE: To formulate and evaluate herbal sunscreen with determination of Sun Protection Factor (SPF) and anti-oxidant activity. To compare Sun Protection Factor of developed formulation with marketed formulation. METHOD: The formulation was developed according to the prepared formula. And multiple tests were done for e

APA, Harvard, Vancouver, ISO, and other styles

37

Kandukuru Sunil Kumar and Metta Naga Bhargavi. "Formulation and evaluation of triclabendazole nanoparticles." World Journal of Advanced Research and Reviews 19, no. 2 (2023): 504–18. http://dx.doi.org/10.30574/wjarr.2023.19.2.1575.

Full text

Abstract:

The aim of the study is the formulation and evaluation of triclabendazole nanoparticles. There is a need to develop alternative novel drug delivery formulations of Triclabendazole to improve its intestinal absorption and also reduce its side effects during regular therapy. The Triclabendazole nanoparticles were prepared by hot homogenization method under high magnetic stirring using stearic acid as lipid, and poloxamer 188 was used as a surfactant. Initial pre-formulation studies using FTIR spectroscopy reveal no interactions between Triclabendazole and other excipients; hence, they can be use

APA, Harvard, Vancouver, ISO, and other styles

38

Kandukuru, Sunil Kumar, and Naga Bhargavi Metta. "Formulation and evaluation of triclabendazole nanoparticles." World Journal of Advanced Research and Reviews 19, no. 2 (2023): 505–18. https://doi.org/10.5281/zenodo.10839601.

Full text

Abstract:

The aim of the study is the formulation and evaluation of triclabendazole nanoparticles. There is a need to develop alternative novel drug delivery formulations of Triclabendazole to improve its intestinal absorption and also reduce its side effects during regular therapy. The Triclabendazole nanoparticles were prepared by hot homogenization method under high magnetic stirring using stearic acid as lipid, and poloxamer 188 was used as a surfactant. Initial pre-formulation studies using FTIR spectroscopy reveal no interactions between Triclabendazole and other excipients; hence, they can be use

APA, Harvard, Vancouver, ISO, and other styles

39

Dhananjay, Patil Momin Sanaurrehman* Vinod Bairagi Abdurrahman Mohammed Awais Shrivastav Karishma Rajashri More. "FORMULATION DEVELOPMENT AND EVALUATION OF FAMCICLOVIR ORALLY DISINTEGRATING TABLET." INDO AMERICAN JOURNAL OF PHARMACEUTICAL SCIENCES 05, no. 09 (2018): 8427–39. https://doi.org/10.5281/zenodo.1411930.

Full text

Abstract:

Orally disintegrating systems have an edge amongst the oral drug delivery systems due to the highest component of compliance they enjoy in patients especially the geriatrics and pediatrics. In addition, patients suffering from dysphagia, motion sickness, repeated emesis and mental disorders prefer these medications because they cannot swallow large quantity of water. Further, drugs exhibiting satisfactory absorption from the oral mucosa or intended for immediate pharmacological action can be advantageously formulated in these dosage forms. However, the requirements of formulating these dosage

APA, Harvard, Vancouver, ISO, and other styles

40

Thombre, Nilima A., Pooja S. Niphade, Eknath D. Ahire, and Sanjay J. Kshirsagar. "Formulation Development and Evaluation of Microemulsion Based Lornoxicam Gel." Biosciences Biotechnology Research Asia 19, no. 1 (2022): 69–80. http://dx.doi.org/10.13005/bbra/2968.

Full text

Abstract:

The objective of the existing research was formulation development and preparation of microemulsion loaded emulgel in augmenting the topical delivery of Lornoxicam. Emulsion and gel combined are recognized as Emulgels. Gelling agents Carbopol 940, 974, 980 were used to formulating Lornoxicam emulgel. The drug release from emulgel was determined depending on the different gelling agents. Clove oil for internal phase and Polyethylene glycol 200 was applied as co-surfactant and Tween 20 as permeation enhancer. Prepared emulgels were evaluated for in-vitro and in- vivo anti-inflammatory activity u

APA, Harvard, Vancouver, ISO, and other styles

41

Dr., Dilip Agrawal, Rakesh Goyal Dr., Mukesh Bansal Dr., Ashok Kumar Sharma Mr., Mohit Khandelwal Mr., and Shaneza Aman Ms. "DEVELOPMENT AND EVALUATION OF ECONAZOLE ORGANOGEL." International Journal of Current Pharmaceutical Review and Research 13, no. 2 (2021): 15–23. https://doi.org/10.5281/zenodo.12667254.

Full text

Abstract:

The main purpose of this study was to develop a topical drug delivery (Organogel) ofEconazole to reduce the dose of the drug, to improve patient compliance, to avoid the sideeffects and increase local onset absorption. Econazole is an imidazole derivative antifungal totreat fungal and protozoal infections. Methods: Topical Organogel formulations ofEconazole were prepared using span-60 with different penetration enhancer with theirdifferent concentrations. Six different formulations of econazole were prepared and evaluatedwith respect to their colour, Spreadability, viscosity parameter, determi

APA, Harvard, Vancouver, ISO, and other styles

42

Sunil Aher, Poonam Patil, Kiran Mahajan, et al. "Formulation and Evaluation of Lornoxicam Nanosuspension with Eudragit Rs100 Polymer." Journal of Advanced Zoology 44, S-5 (2023): 2227–37. http://dx.doi.org/10.17762/jaz.v44is-5.1823.

Full text

Abstract:

BCS Class II has a low aqueous solubility problem in pharmaceutical formulation. Hence to overcome this problem this research the was carried out for BCS Class II drug lornoxicam was selected to enhance the aqueous solubility by formulating nanosuspension with a polymer like Eudragit RL100, Eudragit RS100 and Poloxamber407 as a stabilizer. The present study focuses on the polymer Eudragit RS100. A total of four formulations LRS-F1, LRS-F2, LRS-F3, LRS-F4, and LRS-F4 were prepared with a ratio of drug: polymer: stabilizer (1:1:0.5 & 1:2:0.5, 1:1:1 & 1:2:1)LRS-F4 formulation was found to

APA, Harvard, Vancouver, ISO, and other styles

43

Vydehi, Maheshwaram* Alekya Muduthanapally. "PREPARATION AND EVALUATION OF EXTENDED RELEASE TABLETS OF VENLAFAXINE HYDROCHLORIDE." Indo American Journal of Pharmaceutical Sciences (IAJPS) 03, no. 09 (2016): 1043–48. https://doi.org/10.5281/zenodo.157816.

Full text

Abstract:

The present investigation is aimed at formulating and evaluating Extended release tablets of Venlafaxine Hcl using different polymers such as HPMC K4M, Eudragit RL-100.Venlafaxine Hydrochloride used for the management of major depressive disorder. Different concentrations of the polymers were taken. The physical mixture was evaluated prior to compression for determining the flow properties. These tablets were evaluated for weight variation, hardness, thickness, friability, content uniformity and in-vitro drug release profile. It was found that the formulation F3 containing HPMC K4M Polymer rel

APA, Harvard, Vancouver, ISO, and other styles

44

Kumar, Sagar1* Painuly Neelam2. "Formulation And Evaluation Of Herbal Analgesic Cream." International Journal in Pharmaceutical Sciences 2, no. 7 (2024): 258–69. https://doi.org/10.5281/zenodo.12657970.

Full text

Abstract:

Herbal analgesic creams offer a promising avenue for natural pain relief, leveraging the therapeutic properties of botanical ingredients. This formulation is developed using standard formulation of herbal analgesic cream, each varying in the ratio of key ingredients to optimize efficacy. Turmeric, ginger, arnica, lemon balm, and liquorice were selected for their well-documented analgesic and anti-inflammatory properties. The formulations were prepared using a meticulous process, ensuring the integration of active ingredients with suitable excipients for stability and skin compatibility. The me

APA, Harvard, Vancouver, ISO, and other styles

45

Manish Wani, Akshay Baheti, Satish Polshettiwar, Tanaji Nandgude, Aarti Shastri, and Yogita Ozarde. "Design and Evaluation of Flurbiprofen Micro-Emulsion Based Gel." International Journal of Research in Pharmaceutical Sciences 11, no. 4 (2020): 7293–300. http://dx.doi.org/10.26452/ijrps.v11i4.3868.

Full text

Abstract:

Flurbiprofen via oral route has many side effects. Many inflammatory infections occur locally and close to the body's surface, so topical application of flurbiprofen is advantageous. Still, intact skin acts as a barrier and hampers skin penetration of the drug. Present objective of this work was to reduce the adverse effect of flurbiprofen and increase its bioavailability by formulating Flurbiprofen microemulsion based gel, evaluating it for its Physico-chemical properties and then finally conducting its in-vitro and animal studies to determine its efficiency. Arachis oil was selected as an oi

APA, Harvard, Vancouver, ISO, and other styles

46

Hemamalini, Saravanan K. L. Senthil Kumar. "Formulation And Evaluation Of Medicated Chewing Gum Containing Metformin And Glimepiride." International Journal of Pharmaceutical Sciences 2, no. 4 (2024): 503–20. https://doi.org/10.5281/zenodo.10943964.

Full text

Abstract:

The formulation and evaluation of MCG containing a combination of anti-diabetic drugs is a critical endeavor in pharmaceutical research, aiming to enhance drug efficacy and patient compliance in managing diabetes mellitus. Combining anti-diabetic drugs in a single formulation offers potential advantages such as synergistic effects, improved glycemic control and simplified dosing regimens. Micro-crystalline cellulose, a widely used pharmaceutical excipients, can serve as an ideal matrix for such formulations due to its inert nature, high surface area and excellent compressibility properties. Th

APA, Harvard, Vancouver, ISO, and other styles

47

Shilakari Asthana, Gyati, Abhay Asthana, Davinder Singh, and Parveen Kumar Sharma. "Etodolac Containing Topical Niosomal Gel: Formulation Development and Evaluation." Journal of Drug Delivery 2016 (July 11, 2016): 1–8. http://dx.doi.org/10.1155/2016/9324567.

Full text

Abstract:

The present study aimed to investigate the delivery potential of Etodolac (ETD) containing topical niosomal gel. Niosomal formulations were prepared by thin film hydration method at various ratios of cholesterol and Span 60 and were evaluated with respect to particle size, shape, entrapment efficiency, and in vitro characteristics. Dicetyl phosphate (DCP) was also added in the niosomal formulation. Mean particle size of niosomal formulation was found to be in the range of 2 μm to 4 μm. Niosomal formulation N2 (1 : 1) ratio of cholesterol and surfactant displayed good entrapment efficiency (96.

APA, Harvard, Vancouver, ISO, and other styles

48

Raziya, Begum Sheikh. "Development and Assessment of Naproxen Mouth Dissolving Tablets." medtigo Journal of Pharmacology 1, no. 1 (2024): e13377773. https://doi.org/10.5281/zenodo.13377773.

Full text

Abstract:

The market demand for orally disintegrating tablets has experienced a significant surge over the past decade. This intervention is particularly beneficial for geriatric and pediatric patients who experience challenges in ingesting traditional tablets and capsules. The utilization of a fast dissolving or fast disintegrating dosage form confers advantages to patients in this context. Fast dissolvable or fast disintegrating dosage forms are designed to rapidly disintegrate upon exposure to saliva, resulting in accelerated drug release within the oral cavity. The administration of fast-disintegrat

APA, Harvard, Vancouver, ISO, and other styles

49

Nikam, Shreya. "ANTI-ACNE GEL OF ISOTRETINOIN: FORMULATION AND EVALUATION." Asian Journal of Pharmaceutical and Clinical Research 10, no. 11 (2017): 257. http://dx.doi.org/10.22159/ajpcr.2017.v10i11.19614.

Full text

Abstract:

Objective: Isotretinoin is a very effective drug in the treatment of acne vulgaris by topically. The objective of present study was formulation development of anti-acne gel using Isotretinoine and span 80 for topical delivery to cure nodulosystic acne vulgaris. Furthermore, the comparative study of all the evaluation parameters done with marketed formulation of same drug.Methods: Formulation of anti-acne gel of isotretinoin using Carbopol 940 as a polymer and incorporating isotretinoin in form of topical semi-solid gel using magnetic stirrer, Cremophor RH 40, and butylated hydroxytoluene. Drug

APA, Harvard, Vancouver, ISO, and other styles

50

Saurabh, Gupta* Dilip Kumar Chanchal and Surabhi Rashi. "FORMULATION AND EVALUATION OF CLINDAMYCIN PHOSPHATE EMULGEL." Indo American Journal of Pharmaceutical Sciences 04, no. 11 (2017): 4071–77. https://doi.org/10.5281/zenodo.1045473.

Full text

Abstract:

<strong><em>Introduction:</em></strong><em> Topical drug administration is simplest and easiest route of localized drug delivery anywhere in the body by routes as ophthalmic, rectal, vaginal and skin. These are applied as wide spectrum of preparations in case of both cosmetic and dermatological, to the healthy or diseased skin. Drugs are administered topically for their action at the site of application or for systemic effects. Clindamycin is a lincosamide antibiotic. It is usually used to treat infections with anaerobic bacteria, but can also be used to treat some protozoal diseases, such as

APA, Harvard, Vancouver, ISO, and other styles

We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!