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Thematische Bibliographien / Formulation / Zeitschriftenartikel

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Zeitschriftenartikel zum Thema „Formulation“

Autor: Grafiati

Veröffentlicht am 4. Juni 2021

Zuletzt aktualisiert am 25. Juli 2025

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1

Fernando, Irosh, and Mahesh Rajasooriya. "Case formulation using Pattern-based Formulation (PBF) methodology: clinical case 2." Australasian Psychiatry 26, no. 1 (2017): 65–69. http://dx.doi.org/10.1177/1039856217737885.

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Objectives: To teach psychiatric case formulation; to build a repertoire of patterns that can be reused as building blocks in constructing case formulations. Method: Pattern-based Formulation. Results: Demonstration of a case formulation and introducing three patterns. Conclusion: The demonstration will assist learning case formulation using the Pattern-based Formulation, while the three patterns introduced can be reused when formulating relevant cases.

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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 s

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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 <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

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Buruju Vennela, Arumugam Siva Kumar, Kassa Jyothi, and Arumugam Yasodha. "Development and characterization of Decitabine Niosomes." World Journal of Biology Pharmacy and Health Sciences 19, no. 1 (2024): 382–92. http://dx.doi.org/10.30574/wjbphs.2024.19.1.0445.

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The present study was focused on formulating and evaluating Decitabine containing niosomes formulation for In Vitro studies. Niosomal formulations were prepared by using different ratio of surfactant (Tween 80 and Tween 20) and cholesterol by thin film hydration method and were evaluated for In Vitro characteristics, stability studies. Span 20 containing niosomal formulation displayed highest entrapment efficiency with desired particle size. SEM analyses showed that niosomal formulation was spherical in shape. Niosomes containing Tween 20 displayed higher percentage of drug release after 8 h a

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Buruju, Vennela, Siva Kumar Arumugam, Jyothi Kassa, and Yasodha Arumugam. "Development and characterization of Decitabine Niosomes." World Journal of Biology Pharmacy and Health Sciences 19, no. 1 (2024): 382–92. https://doi.org/10.5281/zenodo.13789911.

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The present study was focused on formulating and evaluating Decitabine containing niosomes formulation for <em>In Vitro </em>studies. Niosomal formulations were prepared by using different ratio of surfactant (Tween 80 and Tween 20) and cholesterol by thin film hydration method and were evaluated for <em>In Vitro </em>characteristics, stability studies. Span 20 containing niosomal formulation displayed highest entrapment efficiency with desired particle size. SEM analyses showed that niosomal formulation was spherical in shape. Niosomes containing Tween 20 displayed higher

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Djunaedy, Achmad, Syaiful Khoiri, Dheananda Fyora Hermansyah Azari, et al. "Development of Bacillus thuringiensis-based liquid and paste formulations for controlling invasive pest species Spodoptera frugiperda J. E. Smith." Jurnal Hama dan Penyakit Tumbuhan Tropika 24, no. 2 (2024): 154–61. http://dx.doi.org/10.23960/jhptt.224154-161.

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Spodoptera frugiperda J.E. Smith (Spodoptera: Noctuidae) is an invasive pests of maize that has been reported around the world. Control efforts using biological agents continue to be developed, including the use of entomopathogen bacteria such as Bacillus thuringiensis. To boost the efficacy and efficiency of biological control, formulations are required. The objective of this study was to develop biopesticide formulations and evaluate their efficacy. The research was carried out by formulating B. thuringiensis strain BtJ2 (1010 cfu mL -1) in liquid and paste formulations. The effectiveness of

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Djunaedy, Achmad, Syaiful Khoiri, Dheananda Fyora Hermansyah Azari, et al. "Development of Bacillus thuringiensis-based liquid and paste formulations for controlling invasive pest species Spodoptera frugiperda J. E. Smith." Jurnal Hama dan Penyakit Tumbuhan Tropika 24, no. 2 (2024): 158–65. http://dx.doi.org/10.23960/jhptt.224158-165.

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Spodoptera frugiperda J.E. Smith (Spodoptera: Noctuidae) is an invasive pests of maize that has been reported around the world. Control efforts using biological agents continue to be developed, including the use of entomopathogen bacteria such as Bacillus thuringiensis. To boost the efficacy and efficiency of biological control, formulations are required. The objective of this study was to develop biopesticide formulations and evaluate their efficacy. The research was carried out by formulating B. thuringiensis strain BtJ2 (1010 cfu mL -1) in liquid and paste formulations. The effectiveness of

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Solon, Lílian Grace da Silva, Ana Isabel Maia de Oliveira, Gerlane Coelho Bernardo Guerra, Luiz Alberto Lira Soares, and Aurigena Antunes de Araújo. "Determination of carbamazepine in pharmaceutical formulations." Brazilian Journal of Pharmaceutical Sciences 46, no. 3 (2010): 509–13. http://dx.doi.org/10.1590/s1984-82502010000300014.

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The aim of this study was to evaluate the quality of five different solid formulations of carbamazepine. The reference formulation was Tegretol® 200.00 mg (Novartis) and the others were: generic formulation of carbamazepine 200.00 mg (National Industry), similar formulation of carbamazepine 200.00 mg (National Industry), and two formulations of carbamazepine 200.00 mg acquired from two different compounding pharmacies. The latter consisted of capsules obtained in Natal, the capital city of the Brazilian State of Rio Grande do Norte. The quality of samples was evaluated through physical and phy

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Surini, Silvia, Nurul Isti Amirtha, and Delly Chipta Lestari. "FORMULATION AND EFFECTIVENESS OF A HAND SANITIZER GEL PRODUCED USING SALAM BARK EXTRACT." International Journal of Applied Pharmaceutics 10, no. 1 (2018): 216. http://dx.doi.org/10.22159/ijap.2018.v10s1.48.

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Objective: The objectives of this study were to determine the minimum inhibitory concentration (MIC) of Salam bark extract against Staphylococcusaureus, formulate and evaluate hand sanitizer gels containing Salam bark extract, and determine the effectiveness of the gels against bacteria on thepalms of the hands.Methods: The gel base was optimized by preparing three formulations containing carbomer and triethanolamine at ratios of 0.25%:0.5%, 0.5%:1%,and 0.5%:2%. The best gel formulation was mixed with Salam bark extract. The physical stability of gels containing 4.04% (formulation 1) and 7.77%

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Yano, J. I., and D. Bouniol. "A minimum bulk microphysics." Atmospheric Chemistry and Physics Discussions 10, no. 12 (2010): 30305–45. http://dx.doi.org/10.5194/acpd-10-30305-2010.

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Abstract. Cloud microphysics present extreme complexities, and even under bulk approaches, the formulation tends to be involved. A minimum microphysics is proposed, aimed at applications for geophysical fluid dynamics, by a maximum simplification of a standard bulk formulation. The proposed formulation is also independently derived by a simple phenomenological argument. The formulational structure of the bulk microphysics is also discussed. The autoconversion process formulation is discussed separately in a phenomenological manner, because a formal application of the bulk approach becomes invo

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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

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Shilakari Asthana, Gyati, Parveen Kumar Sharma, and Abhay Asthana. "In VitroandIn VivoEvaluation of Niosomal Formulation for Controlled Delivery of Clarithromycin." Scientifica 2016 (2016): 1–10. http://dx.doi.org/10.1155/2016/6492953.

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The present study was focused on formulating and evaluating clarithromycin (CLR) containing niosomal formulation forin vitroandin vivopharmacokinetic behavior. Niosomal formulations (empty and drug loaded) were prepared by using different ratio of surfactant (various Span grades 20, 40, 60, and 80) and cholesterol by thin film hydration method and were evaluated forin vitrocharacteristics, stability studies, andin vivostudy. Dicetyl phosphate (DCP) was added to the niosomal formulation. Various pharmacokinetic parameters were determined from plasma of male SD rats. Span 60 containing niosomal

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Choudhary, S., Shriya, P. Chauhan, et al. "Herbicidal effects of Withania somnifera L. leaf extract on Cannabis sativa L., Hordeum vulgare L. and Cicer arietinum." Allelopathy Journal 53, no. 1 (2021): 69–82. http://dx.doi.org/10.26651/allelo.j/2021-53-1-1328.

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We identified the phytochemicals in Withania somnifera L, a multipurpose medicinal plant of the Himalayan región using TLC, FTIR and HPLC. Eleven formulations were made by mixing in different ratios of Withania leaf extract, wood ash and distilled wáter. Wood chips and twigs of 3-years old Pinus roxburghii tree were completely burnt till ashes was used as Wood ash. The 11-formulationss were i.e. formulation I (Withania leaf extract 100%)), formulation II (75:25 concentration (Withania leaf extract: Distilled water)), formulation III (50:50 concentration (Withania leaf extract: Distilled water)

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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.

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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

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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

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Suasin, Mikaela Mae, Mikhaela Camille Tanael, Lea Vanessa Jaro, et al. "Preformulation studies of an emulsion containing commercially available argan oil." SciEnggJ 17, Supplement (2024): 374–78. http://dx.doi.org/10.54645/202417supbyp-48.

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Background: Argan oil has gained popularity in recent years due to its potential anti-inflammatory and antioxidant properties. The present pre-formulation study sought to investigate the suitability of using commercially available argan oil as a unique pharmaceutical emulsion formulation for oral consumption. This research aimed to develop an efficient pre-formulation strategy for oil-in-water emulsion containing argan oil and optimize the formulation's optimum stability as a pharmaceutical dosage form. Methods: Various analytical and physical characterization techniques were employed in makin

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Dhiman, Jasmine, and Priya Sharma. "Optimizing Liposomal Drug Delivery for Enhanced Efficacy in Skin Cancer Treatment: A Comprehensive Experimental Investigation." Journal of Drug Delivery and Therapeutics 14, no. 6 (2024): 87–97. http://dx.doi.org/10.22270/jddt.v14i6.6566.

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Skin cancer is a prevalent global health issue, necessitating ongoing research into innovative treatment approaches. This study focuses on assessing the effectiveness of a liposomal formulation to enhance skin cancer treatment and demonstrates its technological viability. A comprehensive literature review establishes the context by examining current skin cancer treatments and the role of liposomal formulations in dermatological therapies. The research objectives are clearly outlined, detailing the liposomal formulation's characteristics and experimental methodologies. Results from the study, i

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Mohd, Hana, Katarzyna Dopierała, Anze Zidar, Amitkumar Virani, and Bozena Michniak-Kohn. "Effect of Edge Activator Combinations in Transethosomal Formulations for Skin Delivery of Thymoquinone via Langmuir Technique." Scientia Pharmaceutica 92, no. 2 (2024): 29. http://dx.doi.org/10.3390/scipharm92020029.

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Abstract: Thymoquinone (TQ), a bioactive compound found in Nigella sativa seeds, possesses diverse therapeutic properties for skin conditions. However, formulating TQ presents challenges due to its hydrophobic nature and chemical instability, which hinder its skin penetration. Transethosomes, as a formulation, offer an environment conducive to enhancing TQ’s solubility, stability, and skin permeation. To optimize TQ transethosomal formulations, we introduced a combination of ionic and nonionic surfactants, namely Tween 20 and sodium lauryl sulfate (SLS) or sodium lauroyl glutamate (SLG). Surfa

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Jesi Pebralia. "PRINSIP KETIDAKPASTIAN HEISENBERG DALAM TINJAUAN KEMAJUAN PENGUKURAN KUANTUM DI ABAD 21." JOURNAL ONLINE OF PHYSICS 5, no. 2 (2020): 43–47. http://dx.doi.org/10.22437/jop.v5i2.9049.

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The Heisenberg uncertainty principle is the basic foundation of quantum physics that characterizes quantum physics with classical physics. The Heisenberg uncertainty principle provides boundaries where there are no absolute measurement results in any quantum measurement. Along with the development of increasingly sophisticated measurement instruments in the 21st century, presents the opportunity for the emergence of modifications from the Heisenberg uncertainty principle from the general form of existing formulations. This study aims to provide an overview of the opportunities for Heisenberg u

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Das, Surajit, Sie Huey Lee, Vernissa Dilys Chia, et al. "Development of microemulsion based topical ivermectin formulations: Pre-formulation and formulation studies." Colloids and Surfaces B: Biointerfaces 189 (May 2020): 110823. http://dx.doi.org/10.1016/j.colsurfb.2020.110823.

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Samata Biswas, N. N. Bala, Sanjiban Utpal Sarkar, and Madhurina Dutta. "Formulation of colloidal astringent solution using green tea and neem oil." World Journal of Biology Pharmacy and Health Sciences 18, no. 2 (2024): 289–302. http://dx.doi.org/10.30574/wjbphs.2024.18.2.0280.

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This thesis explores the formulation of a novel colloidal astringent solution utilizing the synergistic properties of green tea and neem oil in skincare applications. Astringents play a crucial role in skincare, offering benefits such as pore tightening, oil control, and skin texture refinement. Green tea and neem oil, renowned for their antioxidant, anti-inflammatory, and antimicrobial properties, present promising ingredients for enhancing skin health. The study begins with a comprehensive literature review, examining previous research on astringents, green tea, and neem oil. This review elu

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Samata, Biswas, N. Bala N., Utpal Sarkar Sanjiban, and Dutta Madhurina. "Formulation of colloidal astringent solution using green tea and neem oil." World Journal of Biology Pharmacy and Health Sciences 18, no. 2 (2024): 289–302. https://doi.org/10.5281/zenodo.13743850.

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This thesis explores the formulation of a novel colloidal astringent solution utilizing the synergistic properties of green tea and neem oil in skincare applications. Astringents play a crucial role in skincare, offering benefits such as pore tightening, oil control, and skin texture refinement. Green tea and neem oil, renowned for their antioxidant, anti-inflammatory, and antimicrobial properties, present promising ingredients for enhancing skin health. The study begins with a comprehensive literature review, examining previous research on astringents, green tea, and neem oil. This review elu

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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.

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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

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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.

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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

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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 Tra

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Dr. Payal N. Vaja, Dr Payal N. Vaja, and Mr Uttamkumar V. Rakholiya Mr. Uttamkumar V. Rakholiya. "Formulation and Optimization of Fast Dissolving Tablets of Omeprazole Using Design of Experiments (DoE) Approach." International Journal of Pharmaceutical Research and Applications 10, no. 3 (2025): 1550–61. https://doi.org/10.35629/4494-100315501561.

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Objective The main objective of this study was to formulate and evaluate fast dissolving tablets of Omeprazole using direct compression and wet granulation methods and to compare their performance based on various physicochemical parameters and compare the drug release profiles of different formulations to identify the most effective formulation for rapid disintegration and maximum drug release. Method Formulations were developed using direct compression method and formulation variables such as superdisintegrant and binder concentrations were optimized using Box-Behnken Design (BBD). The table

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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

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Mounika, P., P. Vishnu, and Abbulu Konde. "Development and characterization of self micro emulsifying drug delivery system of rosavastatin." GSC Biological and Pharmaceutical Sciences 3, no. 1 (2018): 001–10. https://doi.org/10.5281/zenodo.4307465.

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The present study was undertaken to enhance solubility and dissolution rate of rosuvastatin by formulating it as a self -micro emulsifying drug delivery system (SMEDDS). The SMEDDS were prepared by using castor oil and sesame oil as oils, Tween 80 as surfactant and PEG 200 as co-surfactant. The prepared SMEDDS were further evaluated for drug content, thermodynamic stability and <em>in vitro</em> drug release. Among all the formulations the drug release for F2 formulation was 99.70% in 120 min. So it was considered as the optimized formulation. The selected optimized F2 formulation wa

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AOYAMA, SHOGO. "QUANTIZATION OF THE 2d EFFECTIVE GRAVITY IN THE GEOMETRICAL FORMULATION." International Journal of Modern Physics A 07, no. 23 (1992): 5761–79. http://dx.doi.org/10.1142/s0217751x92002623.

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There exist various formulations to discuss the 2d effective gravity: (i) light-cone gauge formulation; (ii) geometrical formulation; (iii) formulation by the constrained WZWN model; and (iv) conformal gauge formulation. In the formulations other than the last one, quantization of the 2d effective gravity is not complete in the sense that either the central charges of both sectors are not known, or one of them is known but not the other. We will provide a thorough argument on quantization of the 2d effective gravity in the formulation (ii). The argument will allow us to complete the quantizati

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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-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

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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.

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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

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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.

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<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

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Indartantri, Khusnul Berty, Noval Noval, and Husda Oktaviannoor. "Formulasi dan Evaluasi Floating System Tablet Difenhidramin HCl Menggunakan Kombinasi Matriks HPMC K4M dan Na. CMC." Jurnal Surya Medika 7, no. 1 (2021): 107–14. http://dx.doi.org/10.33084/jsm.v7i1.2634.

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A floating system tablet was made using HPMC K4M and Na matrices. CMC with the active substance diphenhydramine HCl, which absorption in the stomach. The research aims to determine the effect of a combination of HPMC K4M and Na. CMC matrices are optimal in a floating system formulation. This research used an experimental method with a RAL design. Tablets were made by direct compression and were evaluated. The results were then analyzed statistically using One Way ANOVA. The loss results on the drying test, the tapped density test, and the measurement of the angle of repose of all formulations

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Pogoda, M. K., D. J. Pree, and D. B. Marshall. "Effects of encapsulation on the toxicity of insecticides to the Oriental fruit moth (Lepidoptera: Tortricidae) and the predator Typhlodromus pyri (Acari: Phytoseiidae)." Canadian Entomologist 133, no. 6 (2001): 819–26. http://dx.doi.org/10.4039/ent133819-6.

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AbstractWe assessed the effects of microencapsulation on the toxicity of chlorpyrifos, cypermethrin, and lambda-cyhalothrin to larvae of the Oriental fruit moth, Grapholita molesta (Busck), in the laboratory and the field. We also compared the toxicity of microencapsulated and traditional formulations to pyrethroid-susceptible and pyrethroid-resistant populations of the predaceous mite Typhlodromus pyri Scheuten in the laboratory. In laboratory bioassays with neonate larvae of G. molesta, the microencapsulated formulations of chlorpyrifos and cypermethrin were less toxic than the wettable-powd

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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.

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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

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Sajjad Qaisar, Masood-ur-Rehman Aarbi, Shahiq-uz-Zaman, Ammar Sadiq, and Talha Rafique. "Formulation development and characterization of famotidine dry suspension for oral use." Journal of Contemporary Pharmacy 6, no. 2 (2022): 49–56. http://dx.doi.org/10.56770/jcp2022622.

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Famotidine an H2 receptor blocker is generally used to treat ulcers of stomach and intestine. Famotidine is available in liquid suspension that is unstable during shelf life. Degradation of the drug as well as bad smell and color change is major problem in liquid suspension. This problem may be solved by formulating the drug as a dry suspension. We prepared four different formulations of famotidine as dry suspension. Geometric mixing methodology was followed to prepare the formulations. IR-spectroscopy showed no incompatibility between excipients used and API. Tests performed to evaluate formu

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Adesigbin, A.J., M.A. Adedeji, M.O. Oyeleke, and O.B. Ologunye. "Binding properties of starch and bentonite in the briquetting of fine particulate charcoal." European Journal of Advances in Engineering and Technology 5, no. 10 (2018): 782–90. https://doi.org/10.5281/zenodo.10726210.

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<strong>ABSTRACT</strong> The main objective of this study is to determine the possibility and to what extent the manufacture of briquettes from slack or charcoal fines may succeed commercially under the conditions existing in Nigeria. The need for Charcoal briquette is of utmost importance in this contemporary world. Data available on the binding properties of starch and bentonite in the briquetting of fine particulate charcoal is very limited. In this study different percentage compositions of the materials such as charcoal fine, sawdust, limestone, cassava starch, borax and bentonite were u

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Mehta, L. Sonali, D. V. Gowda, N. Vishal Gupta, and Manohar M. "FORMULATION AND DEVELOPMENT OF LENALIDOMIDE LOADED DELAYED RELEASE MINI TABLETS IN CAPSULES." International Journal of Applied Pharmaceutics 10, no. 5 (2018): 239. http://dx.doi.org/10.22159/ijap.2018v10i5.26658.

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Objective: Formulation and development of delayed release mini tablets in the capsule of drug lenalidomidein terms of dissolution and stability was the objective of the present work.Methods: Tablets of less than or equal to 3 millimetres diameter are Mini-tablets, which were filled into a capsule. Direct compression method using multi-tip punch was used for compression and coated with eudragit L100 as a seal coating material and with eudragit L30D55 as an enteric coating material was done. Different formulations were prepared and subjected for evaluation like weight variation, hardness, friabi

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Chono, Sumio, Megumi Matsui, Katsuki Nakamura, and Ryoya Kasai. "Ingestibility and Formulation Quality of Lansoprazole Orally Disintegrating Tablets." Journal of Pharmaceutics 2016 (December 1, 2016): 1–6. http://dx.doi.org/10.1155/2016/6131608.

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Objectives. We evaluated the ingestibility and formulation quality of one branded (formulation A) and five generic (formulations B, C, D, E, and F) lansoprazole orally disintegrating (OD) tablets. Methods. Ingestibility, including the oral disintegrating time, taste, mouth feeling, and palatability, was examined by sensory testing in healthy subjects. Formulation qualities, including salivary stability, gastric acid resistance, and intestinal dissolution behavior, were examined. Results and Discussion. The oral disintegration time of formulation F (52 s) was significantly longer than that of o

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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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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.

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<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

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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.

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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

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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.

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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 (

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Ramadhani, Diah, and Nabilla Widiyanti. "Pengaruh Formulasi Serum Nanoemulgel Terhadap Aktivitas Antioksidan Ekstrak Daun Kelor." Jurnal Syntax Fusion 2, no. 08 (2022): 714–29. http://dx.doi.org/10.54543/fusion.v2i08.214.

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Moringa leaves (Moringa oleifera L.) are a good source of natural antioxidants because they contain flavonoids. The purpose of this study was to determine whether Moringa leaf extract can be formulated into nanoemulgel serum preparations, and to see the effect of nanoemulgel serum formulations on antioxidant activity. This research begins with the manufacture of extracts using the maceration method, followed by the manufacture of nanoemulsions. The nanoemulsion consisted of 3 formulations with different Moringa leaf extract, namely the formulation of 1 0.1 g, formulation 2 0.2 g, and formulati

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Weyer, Janelle, Xianzhang Meng, Lynda Finis, Bill Strickland, CheolHee Park, and Seong Jang. "Phase 1, randomized, open-label, single-dose, crossover study to evaluate the bioequivalence of four formulations of oral rivoceranib tablets in healthy subjects." Journal of Clinical Oncology 41, no. 16_suppl (2023): e15122-e15122. http://dx.doi.org/10.1200/jco.2023.41.16_suppl.e15122.

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e15122 Background: Rivoceranib is a novel oral tyrosine kinase inhibitor that potently and selectively inhibits VEGFR2. Rivoceranib is being investigated for indications targeted towards solid malignancies as either monotherapy or in combination with other anticancer therapies. Herein, we assessed the bioequivalence of a single dose of rivoceranib administered as 4 different formulations in healthy subjects. Methods: This single-center, open-label, randomized, single-dose, 4-way crossover study evaluated the bioequivalence of 4 different formulations of rivoceranib oral tablets in healthy adul

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M, Senthilkumar, Pazhanisamy M, and Sathyaseelan V. "EFFICACY OF OIL AND GRANULAR BASED FORMULATIONS OF ENTOMOPATHOGENIC FUNGI, ZOOPHTHORA RADICANS AGAINST THE BIOLOGY OF RICE LEAF FOLDER, CNAPHALOCROCIS MEDINALIS." Journal of Biopesticides 12, no. 02 (2019): 139–44. http://dx.doi.org/10.57182/jbiopestic.12.2.139-144.

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ABSTRACT Experiment was conducted to know the effect of oil and granular based formulations of entomopathogenic fungi, Zoophthora radicans against the biology of rice leaf folder, Cnaphalocrocis medinalis. Among the different formulations of Zoophthora radicans, the highest larval mortality, pupal mortality, adult mortality and the lowest pupal formation and adult emergence was noticed in Z. radicans + Sunflower oil + Glycerol treatment in oil formulation and 81.3 spores/mm2 concentration of granular formulation. The lowest larval mortality, pupal mortality and adult mortality were noticed in

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Hernawan, Hernawan, Septi Nurhayati, Khoirun Nisa, A. W. Indrianingsih, Cici Darsih, and Muhammad Kismurtono. "FORMULATION AND IN VITRO STUDY OF PROPRANOLOL HYDROCHLORIDE CONTROLLED RELEASE FROM CARBOXYMETHYL CHITOSAN-BASED MATRIX TABLETS." Indonesian Journal of Chemistry 13, no. 3 (2013): 242–47. http://dx.doi.org/10.22146/ijc.21283.

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Formulation and in vitro study of propranolol hydrochloride controlled release from carboxymethyl chitosan-based matrix tablets have been conducted. Formulations with various concentrations of carboxymethyl chitosan 2% (F1), 4% (F2), 6% (F3) were done by wet granulation method. Compatibility test was conducted by XRD and FTIR spectroscopy to determine interaction between propranolol hydrochloride and polymer excipients. Dissolution profiles was obtained through in vitro tests release using simulated gastric fluid (without enzymes, pH 1.2) for the first 2 h and followed by simulated intestinal

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Anvy Aditya Raksesi, Ani Intiyati, Melina Sari, and Mujayanto. "Acceptance Test And Fiber Levels Of Red Bean Ice Cream As An Alternative Snack For Obesity Prevention In Adolescent." Journal of Nutrition Explorations 1, no. 2 (2023): 51–59. http://dx.doi.org/10.36568/jone.v1i2.181.

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Obesity is a pathological state. According to the 2019 AKG, adolescent fiber needs are 37 grams. If snacks are given 10% of the need, then 3.7 grams are obtained per snack. To meet this need, an innovative high-fiber snack is made by formulating red beans into ice cream. The aim is to determine the acceptability and fiber content in red bean ice cream products as an alternative snack to prevent obesity. The research method was an experiment on 4 different formulations with a ratio of skimmed milk and red beans 100 : 0 g, 50 : 50 g, 70 : 30 g , 60 : 40 g then an acceptability test was carried o

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Windras Mara, Setyo Tri, Achmad Pratama Rifai, and Rachmadi Norcahyo. "ON DIFFERENT FORMULATIONS FOR THE MULTI-PERIOD VEHICLE ROUTING PROBLEM WITH SIMULTANEOUS PICKUP AND DELIVERY." ASEAN Engineering Journal 13, no. 1 (2023): 27–39. http://dx.doi.org/10.11113/aej.v13.17888.

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In this paper, we extend the vehicle routing problem with simultaneous pickup and delivery (VRPSPD) with a consideration of multiple planning horizons. We propose three alternative mathematical formulations for Periodic-VRPSPD (P-VRPSPD) based on the available formulations for VRPSPD in the literatures, namely the three-index commodity flow formulation, four-index commodity flow formulation, and three-index vehicle flow formulation. We perform comparison analysis by conducting extensive numerical experiments on a set of instances with various complexities in order to evaluate the performance o

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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.

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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

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