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Journal articles on the topic 'Eudragit RLPO'

Author: Grafiati

Published: 2 June 2025

Last updated: 31 July 2025

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1

Bithi, Farzana Akter, Tushar Saha, Nusrat Ahmed, Ikramul Hasan, and Md Selim Reza. "Preparation and In vitro Evaluation of Mucoadhesive Tablets of Montelukast Sodium." Bangladesh Pharmaceutical Journal 20, no. 2 (2018): 123–31. http://dx.doi.org/10.3329/bpj.v20i2.37865.

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Mucoadhesive tablets of montelukast sodium were prepared in order to release the drug for a prolonged period of time so as to reduce the frequency of administration. Direct compression technique was applied using the mucoadhesive polymers which were Methocel K4M CR, Methocel K15M CR, Methocel K100M CR and Eudragit RLPO. Highest percent release of drug after 8 hours was 76% for Methocel K4M CR, 72.13% for Methocel K15M CR, 65.68% for Methocel K100M CR, 65.53% for the combination of Methocel K15M CR and Eudragit RLPO. Higuchi, Krosmeyer-Peppas was the best fitted model for drug release. The Meth

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E., Sathish Reddy Meesala. Srinivasa Rao and Mohammed Ibrahim. "FORMULATION AND IN VITRO, IN VIVO EVALUATION OF CEFADROXIL CONTROLLED GASTRORETENTIVE DRUG DELIVERY SYSTEM." Indo American Journal of Pharmaceutical Sciences 04, no. 07 (2017): 2139–50. https://doi.org/10.5281/zenodo.836461.

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Introduction: Cefadroxil is a first-generation cephalosporin and is very effective against Gram positive and Gram negative infections. Cefadroxil is an antibiotic agent which has high absorption in the upper part of the gastrointestinal tract (GIT). Conventional Cefadroxil tablets produce rapid and relatively high peak blood level and require frequent administration to keep the plasma drug level at an effective range. The present study was carried out with an objective of preparation and in vivo evaluation of floating tablets of using Cefadroxil as a model drug using Eudragit polymers to impro

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3

Imran, Khan, Gaurav Bhaduka Dr., and Dilip Agrawal Dr. "Formulation, Development and Evaluation of Floating Microspheres of Nizatidine for Gastroretentive Drug Delivery." Pharmaceutical and Chemical Journal 12, no. 3 (2025): 1–13. https://doi.org/10.5281/zenodo.15606949.

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Floating microspheres loaded with Nizatidine were prepared using solvent- evaporation method using HPMC, Eudragit RL 100, Eudragit RLPO in different ratio polymers. Drug and polymer in proportion of drug and polymers were dissolved in 1:2 mixture of solvent system of ethanol and dichloromethane. Floating microspheres of Nizatidine were prepared by a solvent diffusion- evaporation method. The nature of polymer influenced the physical characteristics as well as floating behaviour of the microspheres. In vitro buoyancy and in vivo studies confirmed the excellent floating properties of HPMC, Eudra

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Hasan, Ikramul, Shovan Paul, Sharmin Akhter, Navid Jubaer Ayon, and Md Selim Reza. "Evaluation and Optimization of Influence of Permeability Property and Concentration of Polymethacrylic Polymers on Microspheres of Metformin HCl." Dhaka University Journal of Pharmaceutical Sciences 12, no. 2 (2014): 131–41. http://dx.doi.org/10.3329/dujps.v12i2.17611.

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Metformin HCl microspheres were prepared with the aim of increasing its bioavailability and decreasing gastrointestinal side effects by means of sustained action. Eudragit RSPO and Eudragit RLPO, polymers of different permeability characteristics were used to prepare different microspheres. Emulsification solvent evaporation technique using acetone as the internal phase and liquid paraffin as the external phase was the method of choice. Six formulations were prepared using two polymers. The effect of drug loading and polymeric property on the surface morphology, entrapment efficiency, particle

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Ullah, Md Bashir, Md Rezaul Karim, Md Shamsul Alam, Md Rajib Hassan, Mohiuddin Ahmed Bhuiyan, and Md Sohel Rana. "Formulation and In vitro Evaluation of Unfolding Type Expandable Gastroretentive Film of Enalapril Maleate." Bangladesh Pharmaceutical Journal 20, no. 2 (2018): 148–56. http://dx.doi.org/10.3329/bpj.v20i2.37868.

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The present work was based on the development and characterization of unfolding type gastroretentive dosage form appropriate for controlled release of enalapril maleate. Drug loaded films were prepared by solid dispersion technique using methocel K15 and eudragit RSPO and eudragit RLPO as polymers and polyethylene glycol 400 (PEG 400) as the plasticizer. The film folded in a capsule shell was shown to unfold in the gastric juice and provide drug release up to 12 h in the acidic medium. Formulations provided satisfactory unfolding characteristics allowing expansion to remain in the stomach. For

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Saha, Shib Sankar, Mehrina Nazmi, Nandini Saha, and Md Selim Reza. "Preparation and Evaluation of Carbamazepine Sustained Release Tablets." Dhaka University Journal of Pharmaceutical Sciences 11, no. 2 (2013): 173–80. http://dx.doi.org/10.3329/dujps.v11i2.14577.

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The purpose of the present studies was to develop and characterize sustained release tablets of Carbamazepine, an antiepileptic drug. Tablets were prepared by direct compression method. In the formulation, the active drug was taken 200 mg in every formulation. Methocel K4M, Methocel K15M CR, Methocel K100LV CR, Eudragit RSPO and Eudragit RLPO polymers were used as rate retarding agents in twenty four formulations (F-1 to F-24). The effect of hydrophilic polymer PEG 6000 as channeling agent with Methocel K4M was observed in four formulations (F-5 to F-8). The granules were evaluated for angle o

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Kumar, Balagani Pavan, Irisappan Sarath Chandiran, and Korlakunta Narasimha Jayaveera. "Formulation development and evaluation of Glibenclamide loaded Eudragit RLPO microparticles." International Current Pharmaceutical Journal 2, no. 12 (2013): 196–201. http://dx.doi.org/10.3329/icpj.v2i12.17016.

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The objective of the present investigation was to formulate and evaluate microencapsulated Glibenclamide produced by the emulsion solvent evaporation method. Microparticles were prepared using Eudragit RLPO by emulsion solvent evaporation method and characterized for their micromeritic properties, encapsulation efficiency, particle size, drug loading, FTIR, DSC, SEM analysis. In vitro release studies were performed in phosphate buffer (pH 7.4). Stability studies were conducted as per ICH guidelines. The resulting microparticles obtained by solvent evaporation method were free flowing in natu

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8

Verma, P. R. P. "Sustained Release of Theophylline from Eudragit RLPO and RSPO Tablets." Drug Development and Industrial Pharmacy 22, no. 12 (1996): 1243–47. http://dx.doi.org/10.3109/03639049609063244.

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9

Thakur, Nishant, Bhupinder Kaur, Manish Goswami, and Chandan Sharma. "Compatibility studies of the Thiocolchicoside with Eudragit RLPO, Eudragit E100 and Eudragit L100 using thermal and non-thermal methods." Drug Combination Therapy 4, no. 1 (2022): 1. http://dx.doi.org/10.53388/dct2021100301.

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10

Hajba-Horváth, Eszter, Andrea Fodor-Kardos, Nishant Shah, Matthias G. Wacker, and Tivadar Feczkó. "Sustainable Stabilizer-Free Nanoparticle Formulations of Valsartan Using Eudragit® RLPO." International Journal of Molecular Sciences 22, no. 23 (2021): 13069. http://dx.doi.org/10.3390/ijms222313069.

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The bioavailability of the antihypertensive drug valsartan can be enhanced by various microencapsulation methods. In the present investigation, valsartan-loaded polymeric nanoparticles were manufactured from Eudragit® RLPO using an emulsion–solvent evaporation method. Polyvinyl alcohol (PVA) was found to be a suitable stabilizer for the nanoparticles, resulting in a monodisperse colloid system ranging in size between 148 nm and 162 nm. Additionally, a high encapsulation efficiency (96.4%) was observed. However, due to the quaternary ammonium groups of Eudragit® RLPO, the stabilization of the d

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11

Soujanya, B., J. Geethanjali, D. Mounika, and V. Saikishore. "Influence of Casting Solvent and Polymer on Permeability of Propranolol Hydrochloride Through Eudragit RL100 and Eudragit RLPO Films." Research Journal of Pharmaceutical Dosage Forms and Technology 7, no. 1 (2015): 69. http://dx.doi.org/10.5958/0975-4377.2015.00010.5.

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Dr.E, Hari Krishna T. Mallika *. DS Spandana M. Harika Raj S. Jyothi. "DEVELOPMENT AND EVALUATION OF METFORMIN HCL LOADED EUDRAGIT®RSPO AND EUDRAGIT®RLPO AND GLIMEPIRIDE BILAYER TABLETS." Indo American Journal of Pharmaceutical Sciences 04, no. 09 (2017): 3371–80. https://doi.org/10.5281/zenodo.1000995.

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The present study was carried out for developing the formulation of Bilayer tablets of Glimepiride, Metformin HCl. Immediate Release (IR) layer was compressed as direct compression method and Sustained Release (SR) layer blends were compressed by wet granulation method. IR and SR layers were evaluated for pre and post compression studies and all studies were found to be within limits. From dissolution data of Glimepiride Immediate release layer, IR5 formulation was shown maximum drug release at 60 min i.e., 96.4%. Hence IR5was concluded as optimised formulation for IR layer. Sustained layer co

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Sharma, Pooja, Anuj Chawla, and Pravin Pawar. "Design, Development, and Optimization of Polymeric Based-Colonic Drug Delivery System of Naproxen." Scientific World Journal 2013 (2013): 1–12. http://dx.doi.org/10.1155/2013/654829.

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The aim of present investigation deals with the development of time-dependent and pH sensitive press-coated tablets for colon specific drug delivery of naproxen. The core tablets were prepared by wet granulation method then press coated with hydroxypropyl cellulose (HPC) or Eudragit RSPO : RLPO mixture and further coated with Eudragit S-100 by dip immerse method. Thein vitrodrug release study was conducted in different dissolution media such as pH 1.2, 6.8, and 7.4 with or without rat caecal content to simulate GIT conditions. Surface morphology and cross-sectional view of the tablets were vis

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14

Kumari, Satish, Anchal Puri, Dhruv Dev, DN Prasad, and ,. Monika. "A review on polymers in natural or modified form used in sustained release tablet." Journal of Drug Delivery and Therapeutics 9, no. 3-s (2019): 870–73. http://dx.doi.org/10.22270/jddt.v9i3-s.2843.

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Tablet is a solid dosage form which is used to deliver the drug to the body to make pharmacological action. The oral dosage form should disperse into small particles to deliver active ingredients in the body, the disperse time of the dosage form depends on the ingredients which are used in the tablet. To make the tablet disintegrate slow usually sustained release agents are used. The sustained release tablets helps in maintaining the drug concentration in the body for the higher time. In this review article various polymers of natural origin and their modified forms are studied, which can be u

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15

Sultana, Nasreen. "PREPARATION AND CHARACTERIZATION OF METHOCEL K4M, EUDRAGIT RLPO AND PEG 4000 LOADED CARBAMAZEPINE MICROSPHERES." International Journal of Advanced Research 6, no. 7 (2018): 731–42. http://dx.doi.org/10.21474/ijar01/7419.

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16

Pirayavaraporn, Chompak, Thomas Rades, and Ian G. Tucker. "Determination of moisture content in relation to thermal behaviour and plasticization of Eudragit RLPO." International Journal of Pharmaceutics 422, no. 1-2 (2012): 68–74. http://dx.doi.org/10.1016/j.ijpharm.2011.10.028.

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17

Gandhi, Arijit, Sougata Jana, and Kalyan Kumar Sen. "In-vitro release of acyclovir loaded Eudragit RLPO® nanoparticles for sustained drug delivery." International Journal of Biological Macromolecules 67 (June 2014): 478–82. http://dx.doi.org/10.1016/j.ijbiomac.2014.04.019.

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18

Partheniadis, Ioannis, Miltiadis Toskas, Filippos-Michail Stavras, Georgios Menexes, and Ioannis Nikolakakis. "Impact of Hot-Melt-Extrusion on Solid-State Properties of Pharmaceutical Polymers and Classification Using Hierarchical Cluster Analysis." Processes 8, no. 10 (2020): 1208. http://dx.doi.org/10.3390/pr8101208.

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The impact of hot-melt extrusion (HME) on the solid-state properties of four methacrylic (Eudragit® L100-55, Eudragit® EPO, Eudragit® RSPO, Eudragit® RLPO) and four polyvinyl (Kollidon® VA64, Kollicoat® IR, Kollidon® SR, and Soluplus®) polymers was studied. Overall, HME decreased Tg but increased electrostatic charge and surface free energy. Packing density decreased with electrostatic charge, whereas Carr’s and Hausner indices showed a peak curve dependency. Overall, HME reduced work of compaction (Wc), deformability (expressed as Heckel PY and Kawakita 1/b model parameters and as slope S′ of

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19

Shetty, Amitha, Akhilesh Dubey, Jeshma Chrystle, et al. "Fabrication and in vitro characterization of curcumin film-forming topical spray: An integrated approach for enhanced patient comfort and efficacy." F1000Research 13 (February 22, 2024): 138. http://dx.doi.org/10.12688/f1000research.142860.1.

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Background Curcumin, known for its anti-inflammatory properties, was selected for the developing consumer friendly film forming spray that offers precise delivery of curcumin and and improves patient adherence. Methods An optimized film-forming solution was prepared by dissolving curcumin (1%), Eudragit RLPO (5%), propylene glycol (1%), and camphor (0.5%) in ethanol: acetone (20:80) as the solvent. The solution was filled in a spray container which contained 70% solutions and 30% petroleum gas. In-vitro characterization was performed. Results Potential anti-inflammatory phytoconstituents were

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20

Shivhare, Shubham, Ashutosh Pal Jain, Teena Jain, et al. "Formulation, Development and Characterization of Transdermal Patches of Glipizide." International Journal of Medical Sciences and Pharma Research 8, no. 3 (2022): 1–7. http://dx.doi.org/10.22270/ijmspr.v8i3.47.

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Transdermal patches are innovative drug delivery systems and can be used for achieving efficient systemic effect by passing hepatic first pass metabolism and increasing the fraction absorbed. Like other drugs among the second-generation sulfonylureas, glipizide (GLP) acts by stimulating insulin secretion from pancreatic beta-cells as well as modifying the responsiveness of insulin-sensitive tissues. GLP belongs to biopharmaceutical classification system (BCS) class II and has a low solubility and high permeability. The aim of the current research was to formulate GLP transdermal patches utiliz

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., Yashoda, and Sunita Sonartiya. "Formulation and evaluation of transdermal patches of nitrendipine eudragit RLPO and RSPO using rate controlling polymers." International Journal of Pharmacy and Pharmaceutical Science 4, no. 2 (2022): 52–56. http://dx.doi.org/10.33545/26647222.2022.v4.i2a.88.

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22

Nath, Bipul, and Lila Kanta Nath. "Design, Development, and Optimization of Sterculia Gum-Based Tablet Coated with Chitosan/Eudragit RLPO Mixed Blend Polymers for Possible Colonic Drug Delivery." Journal of Pharmaceutics 2013 (November 25, 2013): 1–9. http://dx.doi.org/10.1155/2013/546324.

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The purpose of this study is to explore the possible applicability of Sterculia urens gum as a novel carrier for colonic delivery system of a sparingly soluble drug, azathioprine. The study involves designing a microflora triggered colon-targeted drug delivery system (MCDDS) which consists of a central polysaccharide core and is coated to different film thicknesses with blends of chitosan/Eudragit RLPO, and is overcoated with Eudragit L00 to provide acid and intestinal resistance. The microflora degradation property of gum was investigated in rat caecal medium. Drug release study in simulated

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23

Muter, Sarah Sabah, and Athmar Dhahir Habeeb. "Preparation and evaluation of gastroretentive floating unfolding film of baclofen." Pharmacia 72 (May 14, 2025): 1–12. https://doi.org/10.3897/pharmacia.72.e147835.

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Baclofen, a muscle relaxant used for severe pain management, has a narrow absorption window limiting its bioavailability. Enhancing its gastric residence time could potentially improve its absorption and effectiveness. Floating drug delivery systems are a promising approach to prolong drug retention in the stomach. This study aimed to develop a floating bilayer film for the sustained release of baclofen. The core of the film was formulated with baclofen, PVP K90, sodium alginate, and PEG 400 as a plasticizer, while the controlled release layer contained Eudragit RS100 or RLPO with different pl

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Ghosh, Bijaya, Arka Chatterjee, Moumita Das Kirtania, and Sankha Chattopadhyay. "Development of Cinnarizine Microballoons by Sequential Optimization and In Vivo Imaging by Gamma Scintigraphy." Current Drug Therapy 15, no. 4 (2020): 369–80. http://dx.doi.org/10.2174/1574885514666191119105908.

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Background: The drug cinnarizine is used in the treatment of vertigo and migraine. The main drawback is its very low water solubility which causes unpredictable bioavailability. Solubility is better in acidic pH. Therefore, gastro-retentive formulation would be beneficial to improve the bioavailability of the drug. Objective: The objective of the study was to prepare floating microballoons of cinnarizine which would float in the gastric fluid and release the drug in a sustained manner. Methods: Microballoons were prepared by diffusion solvent evaporation technique using polymers (Eudragit® S10

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25

Puttegowda, Venkatesh Dinnekere, Roopa Karki, Divakar Goli, Sajal kumar Jha, and Manjunatha Panduranga Mudagal. "Formulation and Pharmacokinetic Evaluation of Microcapsules Containing Pravastatin Sodium Using Rats." Scientifica 2016 (2016): 1–9. http://dx.doi.org/10.1155/2016/7623193.

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Pravastatin Sodium has a cholesterol lowering agent. It has shorter half-life and undergoes first-pass metabolism. Frequent dose is required in case of conventional dosage form. The purpose of the study is to formulate and evaluate microcapsules containing Pravastatin Sodium by complex with cholestyramine resins coated with Eudragit RLPO and Eudragit RSPO polymers for achieving control release. Complexation of drug on resin was carried out by batch method. Microencapsulation was carried out by nonaqueous solvent evaporation method. Pharmacokinetic studies were done by using rats. The intermedi

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Ch. Akhila, Shaik Zareena Begum, and K. Hariprasad. "Formulation development and in vitro evaluation of terbutaline floating tablets." International Journal of Allied Medical Sciences and Clinical Research 12, no. 4 (2024): 551–61. https://doi.org/10.61096/ijamscr.v12.iss4.2024.551-561.

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The present study outlines a systematic approach for designing and development of Terbutaline floatingtablets to enhance the bioavailability and therapeutic efficacy of the drug. Floating tablets of Terbutaline haveshown sustained release thereby proper duration of action at a particular site and are designed to prolong thegastric residence time after oral administration. Different formulations were formulated by using direct compression method. A floating drug delivery system (FDDS) was developed by using sodium bicarbonate asgas-forming agent and HPMC E5, Eudragit RLPO and Sodium carboxy met

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Muter, Sarah Sabah, and Athmar Dhahir Habeeb. "Preparation and evaluation of gastroretentive floating unfolding film of baclofen." Pharmacia 72 (May 14, 2025): 1–12. https://doi.org/10.3897/pharmacia.72.e147835.

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Baclofen, a muscle relaxant used for severe pain management, has a narrow absorption window limiting its bioavailability. Enhancing its gastric residence time could potentially improve its absorption and effectiveness. Floating drug delivery systems are a promising approach to prolong drug retention in the stomach. This study aimed to develop a floating bilayer film for the sustained release of baclofen. The core of the film was formulated with baclofen, PVP K90, sodium alginate, and PEG 400 as a plasticizer, while the controlled release layer contained Eudragit RS100 or RLPO with different pl

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Ansary, Johura, Amit Kumar Chaurasiya, and KM Bashirul Huq. "Formulation and evaluation of metformin HCl floating microspheres." Asian Journal of Medical and Biological Research 1, no. 3 (2016): 396–405. http://dx.doi.org/10.3329/ajmbr.v1i3.26445.

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The purpose of the present investigation was the preparation and evaluation of gastro-retentive floating drug delivery system for anti-diabetic drug metformin hydrochloride that would retain the drug in stomach and continuously release the drug in controlled manner up to a predetermined time leading to improve bioavailability. The microspheres were prepared by oil-in-oil emulsion solvent evaporation technique using ethyl cellulose, methacrylic acid copolymer (Eudragit RS100, Eudragit RSPO and Eudragit RLPO). The dried floating microspheres were evaluated for percentage yield (%), actul drug co

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Pirayavaraporn, Chompak, Thomas Rades, Keith C. Gordon, and Ian G. Tucker. "Quantification of the types of water in Eudragit RLPO polymer and the kinetics of water loss using FTIR." International Journal of Pharmaceutics 458, no. 1 (2013): 90–98. http://dx.doi.org/10.1016/j.ijpharm.2013.10.012.

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Singh, Inderbir, and Vikas Rana. "Iron oxide induced enhancement of mucoadhesive potential of Eudragit RLPO: formulation, evaluation and optimization of mucoadhesive drug delivery system." Expert Opinion on Drug Delivery 10, no. 9 (2013): 1179–91. http://dx.doi.org/10.1517/17425247.2013.790361.

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Shukla, Kavita Varma, Manisha Swamy, and Rekha Pathak. "Formulation, Development and Characterization of Transdermal Patches of Sitagliptin Phosphate." Journal of Drug Delivery and Therapeutics 9, no. 4-s (2019): 408–13. http://dx.doi.org/10.22270/jddt.v9i4-s.3347.

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Sitagliptin is a dipeptidyl peptidase 4-(DPP-4) inhibitor with glucose controlling capabilities that was effectively used for treating diabetes in the past. However, the oral administration of this drug caused such severe side effects that it was removed from the market. Transdermal patches are innovative drug delivery systems and can be used for achieving efficient systemic effect by passing hepatic first pass metabolism and increasing the fraction absorbed. Transdermal patches of Sitagliptin phosphate (SIT) were prepared by the solvent casting evaporation technique using ethyl cellulose: HPM

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KAUR, CHANCHAL DEEP, GYANESH KUMAR SAHU, AJAZUDDIN ., and HARISH SHARMA. "COMPARATIVE STUDY OF HERBAL BIOENHANCER CONTAINING NANO FORMULATION FOR ORAL DELIVERY OF PACLITAXEL: PHARMACOKINETIC AND CYTOTOXICITY ANALYSIS." International Journal of Pharmaceutical Sciences and Drug Research 14, no. 02 (2020): 244–48. http://dx.doi.org/10.25004/ijpsdr.2022.140214.

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Objective: The main objective of this study was to develop novel formulation containing herbal bioenhancer to increase the bioavailability of poorly water-soluble anticancer drug. Material and methods: Paclitaxel (PTX) loaded bioenhancer nanoparticle prepared by Emulsification solvent evaporation method by using Eudragit RLPO as a polymer and to evaluate its in-vivo pharmacokinetics (PK) and cytotoxicity studies The result is reduced oral bioavailability, which limits the use of paclitaxel, a crucial anticancer medication, when taken orally. Though multiple formulation approaches have been tak

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Sahoo, J., P. N. Murthy, S. Biswal, and Manik. "Formulation of Sustained-Release Dosage Form of Verapamil Hydrochloride by Solid Dispersion Technique Using Eudragit RLPO or Kollidon®SR." AAPS PharmSciTech 10, no. 1 (2009): 27–33. http://dx.doi.org/10.1208/s12249-008-9175-0.

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Kumpugdee-Vollrath, Mont, and Mario Helmis. "Controlled Release of Resveratrol and Lignan by Matrix Tableting." Advanced Materials Research 746 (August 2013): 330–36. http://dx.doi.org/10.4028/www.scientific.net/amr.746.330.

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The aim of this research work was to develop the controlled release of two model drugs i.e. water insoluble drug - resveratrol and water soluble drug - lignan by matrix tableting with an eccentric tablet machine. For this purpose different kinds of polymers i.e. Metolose 90 SH-4000® (HMPC), Fetocel RT-N-100® (EC) and Eudragit RLPO® (polymethacrylate) were used. The matrix tablets containing 2 %wt of a model drug which were mixed with 5, 10, 20, 30 and 50 %wt of the polymers mentioned above. In addition, a glidant composed of 1 %wt talc and 1 %wt magnesium stearate as well as a filler Ludipress

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Khattab, Abeer, and Samia Shalaby. "Optimized Ciclopirox-Based Eudragit RLPO Nail Lacquer: Effect of Endopeptidase Enzyme as Permeation Enhancer on Transungual Drug Delivery and Efficiency Against Onychomycosis." AAPS PharmSciTech 19, no. 3 (2017): 1048–60. http://dx.doi.org/10.1208/s12249-017-0917-8.

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Snehalatha, G., and Shailaja Pashikanti. "Enhanced Breast Cancer Treatment Using Orlistat-Loaded Lipid-Polymer Hybrid Nanoparticles: Formulation, Characterization and Evaluation." Journal of Neonatal Surgery 14, no. 7S (2025): 746–59. https://doi.org/10.52783/jns.v14.2493.

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Breast cancer continues to be a significant global health concern, prompting the development of advanced drug delivery systems to improve therapeutic effectiveness and minimize adverse effects. Lipid-polymer hybrid nanoparticles (LPHNPs) offer a promising approach by combining the benefits of both liposomes and polymeric nanoparticles, thereby improving drug solubility, bioavailability, and controlled release. This study aimed to develop and optimize Orlistat-loaded LPHNPs (ORL-LPHNPs) using soya lecithin, Eudragit RLPO, and Tween 80 via nanoprecipitation. Various formulations (LPHNP1-LPHNP8)

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Samanthula, Kumara Swamy, Agaiah Goud Bairi, and CB Mahendra Kumar. "Muco-adhesive buccal tablets of candesartan cilexetil for oral delivery: preparation, in-vitro and ex-vivo evaluation." Journal of Drug Delivery and Therapeutics 11, no. 1-s (2021): 35–42. http://dx.doi.org/10.22270/jddt.v11i1-s.4547.

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Candesartan cilexetil (CC) is an angiotensin II-receptor blocker (ARB). The antihypertensive effect of CC 4-16 mg/day was as great as that of other once-daily dosage regimens. Candesartan cilexetil has high first-pass metabolism and low oral bioavailability. The bioavailability of such drugs may be significantly improved if delivered through the buccal route; hence mucosal delivery is one of the alternative methods of systemic drug delivery. This study’s objective was to develop mucoadhesive buccal tablets of candesartan cilexetil using carbopol-934P, hydroxyl propyl methyl cellulose (HPMC), E

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Tasneem, Farhana, Marzia Alam, and Md Saiful Islam Pathan. "Preparation and Evaluation of Metronidazole Benzoate Periodontal Patches." Bangladesh Pharmaceutical Journal 18, no. 2 (2015): 97–102. http://dx.doi.org/10.3329/bpj.v18i2.24305.

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Periodontitis is a serious gum disease that damages the soft tissue and destroys the bone that supports the teeth. According to WHO, globally 1520% of middle-aged (35-44 years) adults, suffer from severe periodontal (gum) diseases. Metronidazole benzoate is an antibacterial agent prescribed against different diseases including, periodontitis and several other protozoal infestations. The aim of this experiment was to formulate intrapocket periodontal patches of metronidazole benzoate to provide site specific therapeutic activity with very small loading dose. Nine (F1 to F9) formulations of met

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Patel, Vaishali P., Anita P. Patel, and Ashish Shah. "Optimization of amorphous solid dispersion techniques to enhance solubility of febuxostat." Folia Medica 63, no. 4 (2021): 557–68. http://dx.doi.org/10.3897/folmed.63.e55838.

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Febuxostat is a selective inhibitor of xanthine oxidase and belongs to BCS class II drugs having low solubility and high permeability. Solubility is the most important parameter which directly affects dissolution, absorption and bioavailability of the drugs. There are different techniques by which we can improve solubility and dissolution rate of poorly soluble drug. Amorphous solid dispersion is one of the methods which can improve solubility as well as powder characteristics. The aim of the present study was to formulate and optimize various methods of formulating solid dispersion by using v

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Kim, Woojun, Hai V. Ngo, Hy D. Nguyen, et al. "Nanonization and Deformable Behavior of Fattigated Peptide Drug in Mucoadhesive Buccal Films." Pharmaceutics 16, no. 4 (2024): 468. http://dx.doi.org/10.3390/pharmaceutics16040468.

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This study was tasked with the design of mucoadhesive buccal films (MBFs) containing a peptide drug, leuprolide (LEU), or its diverse nanoparticles (NPs), for enhanced membrane permeability via self-assembled nanonization and deformable behavior. An LEU-oleic acid conjugate (LOC) and its self-assembled NPs (LON) were developed. Additionally, a deformable variant of LON (d-LON) was originally developed by incorporating l-α-phosphatidylcholine into LON as an edge activator. The physicochemical properties of LON and d-LON, encompassing particle size, zeta potential, and deformability index (DI),

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Saharan, Priyanka, and Shyo Parakash Saharan. "Designing and Characterization of Docetaxel Loaded Nanoparticles with Piperine." Journal of Pharmaceutical Research International 36, no. 8 (2024): 55–64. http://dx.doi.org/10.9734/jpri/2024/v36i87558.

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Objective: The main objective of this research was to develop a novel formulation with an herbal bioenhancer to boost the bioavailability of an anticancer drug that was poorly soluble in water and overcome its limitations of short half-life. Methods: Eudragit RLPO was used as a polymer in an emulsification solvent evaporation process to generate Docetaxel loaded bioenhancer (Piperine) nanoparticles and to evaluate its parameters. Results: The study demonstrated that encapsulating Docetaxel with herbal bioenhancers (Piperine) in a nanoparticle system effectively enhanced its in vitro release pr

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KAUR, CHANCHAL DEEP, GYANESH SAHU, SWARNALI DAS PAUL, HARISH SHARMA, and AJAZUDDIN . "DESIGN AND CHARACTERIZATION OF PACLITAXEL LOADED NANOPARTICLES WITH PIPERINE." International Journal of Pharmaceutical Sciences and Drug Research 14, no. 02 (2020): 238–43. http://dx.doi.org/10.25004/ijpsdr.2022.140213.

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Objectives: Paclitaxel is a cytotoxic drug having wonderful mechanism against cancer cells. However, it showed severe dose-limiting toxicity when administered as infusion. To overcome these side effects a suitable delivery system is highly desirable. Bioenhancers, when mixed with drugs promote and augment their bioavailability and reduced incidence of drug resistance and risk of adverse drug reaction. Therefore, we selected nanoparticles as a delivery system in this study. The object of this work was to entrap paclitaxel and herbal bioenhancer in a nanoparticle system. Materials and methods: W

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Genç, Lütfi, and A. Kıran. "In Vitro Evaluation of Sustained Released Matrix Tablet Formulations of Clarithromvcin." Scientia Pharmaceutica 73, no. 1 (2005): 59–74. http://dx.doi.org/10.3797/scipharm.aut-05-05.

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Sustained release matrix tablets of clarithromycin were prepared using different polymers as Hydroxypropyl methylcellulose (H PMC), Carbopol 934 and Eudragit RL/PO by direct compression technique. For the quality control of these formulations, weight deviation, hardness, friability, diameter-height ratio, content uniformity of the active substance and in vitro dissolution technique were performed. HPLC was used for the assay of clarithromycin and the assay method was validated. Dissolution profiles of the tablets were plotted and evaluated kinetically. The effects on drug release of polymer ty

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AMIN, MILIND J., KEYUR S. PATEL, DEEPA R. PATEL, ZIL P. PATEL, and JAYANTI V. BAJAG. "FORMULATION AND EVALUATION OF SUSTAINED-RELEASE PELLETS OF LORNOXICAM." International Journal of Applied Pharmaceutics, July 7, 2021, 221–27. http://dx.doi.org/10.22159/ijap.2021v13i4.41601.

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Objective: The aim of the study was to develop sustained release pellets of lornoxicam using Eudragit RLPO and Eudragit RSPO to reduce the dosing frequency. Methods: The sustained release pellets of lornoxicam were prepared by extrusion–spheronization technique using Eudragit RLPO and Eudragit RSPO as release retardant polymers and microcrystalline cellulose as spheronizing agent. A 32 Full factorial design was applied to investigate the combined effect of the two independent variables i.e. concentration of Eudragit RLPO (X1) and concentration of Eudragit RSPO (X2) on the dependent varia

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Venkata, Durga Seshu Priya P., Babu K. Ramesh, Prasad Reddy B. Bhanu, et al. "Formulation Development and Characterization of Glipizide Transdermal Gels by Using Permeation Enhancers." October 9, 2021. https://doi.org/10.26452/fjphs.v1i4.172.

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That in research paper an effort were made to formulate glipizide transdermal patches using different permeation enhancers. The results obtained determined the polymer and solvent victimized had an influence on drug diffusion and permeability of the films. These results obtained showed that the drug diffusion via Eudragit RLPO films was relatively high compared to Eudragit RS100 and Eudragit RL100 films (Eudragit RLPO> Eudragit RL100> Eudragit RS100). The Formulation G6 has shown a good release. The effects designated to the nonionic surfactant Tween 20 expands the permeability qualities

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Dunaboina, Anusha* Mr. D. Appalaraju Mrs. M. Vineela. "FORMULATION AND IN VITRO EVALUATION OF SUSTAINED RELEASE MATRIX TABLETS OF ACECLOFENAC." August 1, 2023. https://doi.org/10.5281/zenodo.8206043.

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<em>The main aim of present work was to formulate and evaluate sustain release matrix tablets of Aceclofenac is a nonsteroidal anti-inflammatory drug (NSAID). Sustain release formulation are those which delivers the drug locally or systemically at a predetermined rate for a fixed period of time. The matrix tablet was prepared by direct compression method using by various concentration of Sodium Alginate and Eudragit RLPO various release retardant polymer. The powder mixtures were subjected to various pre-compression parameters such as angle of repose, bulk density, tapped density and Carr&rsqu

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Daslaniya, Dhiren, Manish Patel, and Amarish Shah. "DESIGN, DEVELOPMENT AND CHARACTERIZATION OF EXTENDED RELEASE MULTIUNIT PARTICULATE SYSTEM OF ANTI-INFLAMMATORY DRUG." International Journal of Pharmaceutical Sciences and Drug Research, July 1, 2009, 100–102. https://doi.org/10.25004/ijpsdr.2009.010209.

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Multi unit particulate system has long been employed to improve the bioavailability of drugs. Mesalamine pellets were prepared by Coating drug solution on sugar sphere followed by various functional coating. The influence of rate controlling membrane made up of Eudragit RSPO and Eudragit RLPO in combination with delay release polymer coating with Eudragit L100 in different proportions on drug release kinetics was studied. Pellets were for the various parameter like Physical characteristics, assay and in-vitro dissolution profile. The study confirmed that mesalamine can be delivered by multi un

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Kikawoos, Haider H., and Athmar DH H. Al-Shohani. "Preparation and evaluation of biodegradable double-layer insert of Sulfacetamide sodium for ocular drug delivery." Palestinian Medical and Pharmaceutical Journal 10, no. 4 (2025). https://doi.org/10.59049/2790-0231.10.4.2411.

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A key challenge in ocular medication administration is attaining a therapeutic drug concentration at the site of action for a prolonged duration. The present study employed the antibacterial Sulfacetamide in a biodegradable ocular insert to achieve prolonged drug release. The inserts were prepared using solvent casting for the matrix and dipping technique for the rate-controlling layer. The polymers utilized were medium-viscosity sodium alginate, polyvinyl pyrrolidine K90, and Eudragit RLPO. All developed inserts were assessed for folding durability, thickness, drug content, swelling capacity,

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Ahuja, Munish, Preeti Chauhan, Rimpy, Pooja Kumari, and Tarun Kumar. "Development and Evaluation of Luliconazole Nail Lacquer Containing Potential Permeation Enhancers for an Enhanced Transungual Drug Delivery." Drug Delivery Letters 13 (November 17, 2022). http://dx.doi.org/10.2174/2210303113666221117085703.

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BACKGROUND: Topical therapy for nail infection has a serious drawback of drug permeation via keratinized human nail plate. Onychomycosis, or tinea unguium, is a human nail fungal infection affecting nearly 19% of the world’s population. AIM: Purposely, we aimed to develop and evaluate nail lacquer formulations incorporated with luliconazole utilizing different permeation enhancers for targeted transungual drug delivery. Nail clippings were treated with luliconazole solution (5% w/v) with or without permeation enhancers and screened by determining the hydration enhancement factor and retention

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K. Deepika, M. Sai Vishnu, and A. Lakshmana Rao. "Development and Evaluation of Controlled Release Formulations of Esomeprazole." International Journal of Research in AYUSH and Pharmaceutical Sciences, December 26, 2021, 536–52. http://dx.doi.org/10.47070/ijraps.v5i5.115.

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The present work was aimed to development of controlled release formulations of Esomeprazole to improve bioavailability. Esomeprazole is the proton pump inhibitor that suppresses gastric acid secretion by specific inhibition of the H+/K+-ATPase in the gastric parietal cell. By acting specifically on the proton pump, Esomeprazole blocks the final step in acid production, thus reducing gastric acidity. Construction of calibration curve of Esomeprazole and to investigate the drug and polymer interaction studies by FTIR and DSC. To prepare the different controlled release formulations of Esomepraz

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