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Relevant bibliographies by topics / Eudragit RSPO

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Journal articles

Academic literature on the topic 'Eudragit RSPO'

Author: Grafiati

Published: 3 June 2025

Last updated: 31 July 2025

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Journal articles on the topic "Eudragit RSPO"

1

Cetin, Meltem, Alptug Atila, Selma Sahin, and Imran Vural. "Preparation and characterization of metformin hydrochloride loaded-Eudragit®RSPO and Eudragit®RSPO/PLGA nanoparticles." Pharmaceutical Development and Technology 18, no. 3 (2011): 570–76. http://dx.doi.org/10.3109/10837450.2011.604783.

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2

Tagami, Tatsuaki, Maya Okamura, Koki Ogawa, and Tetsuya Ozeki. "Fabrication of Mucoadhesive Films Containing Pharmaceutical Ionic Liquid and Eudragit Polymer Using Pressure-Assisted Microsyringe-Type 3D Printer for Treating Oral Mucositis." Pharmaceutics 14, no. 9 (2022): 1930. http://dx.doi.org/10.3390/pharmaceutics14091930.

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Oral mucositis in the oral cavity, caused by radiation therapy and chemotherapy, requires personalized care and therapy due to variations in the lesions of patients. In the present study, we fabricated a model of personalized oral film containing an ibuprofen/lidocaine ionic liquid (IL) for patients with oral mucositis using a pressure-assisted microsyringe-type 3D printer at room temperature. The film contained a Eudragit polymer (L100, EPO, or RSPO) to make the film solid, and the printer ink was composed of organo ink (organic solvent to dissolve both drugs and the Eudragit polymer). The vi

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3

Sanghai, Piyush, Tanaji Nandgude, and Sushilkumar Poddar. "Formulation of Bilayer Benzydamine HCl Patch Targeted For Gingivitis." Journal of Drug Delivery 2016 (December 29, 2016): 1–9. http://dx.doi.org/10.1155/2016/7598398.

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In the present study bilayer patch of benzydamine HCl was developed using solvent casting method. Different substrates were attempted like Petri dish, glass-and-ring, and teflon-and-ring for selection of the proper option to formulate patch that should give easily peelable film with adequate mechanical properties. HPMC E15 LV was used in different concentrations for obtaining proper viscosity of solution for pouring on to surface and ring, that it should not leak from ring. The second layer was optimized by using different polymer like eudragit RSPO, eudragit RSPO + EC, and eudragit NE30 D for

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4

Thireesha, Bannaravuri, Ayya Rajendra Prasad, and Haroled Peter P L. "FORMULATION AND EVALUATION OF LORNOXICAM MICROSPONGES USING EUDRAGIT RS 100 AND EUDRAGIT RSPO." Asian Journal of Pharmaceutical and Clinical Research 11, no. 10 (2018): 217. http://dx.doi.org/10.22159/ajpcr.2018.v11i10.26861.

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Objective: The objective of the present study was preparation and evaluation of lornoxicam microsponges to prolong their drug release up to 12 h for effective osteoarthritis, rheumatoid arthritis, and acute lumbar-sciatica therapy.Methods: Lornoxicam microsponges were prepared by the quasi-emulsion solvent diffusion technique using different concentrations of polymers such as Eudragit RS 100 and Eudragit RSPO in ethanol and dichloromethane organic solvent mixture. Microsponges were evaluated for their particle size, percentage yield, entrapment efficiency, scanning electron microscopy (SEM), a

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5

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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6

Akhter, Sharmin, Shova Paul, Ikramul Hasan, Navid Jubaer Ayon, Syed Shabbir Haider, and Md Selim Reza. "Preparation, Characterization and Compatibility Studies of Naproxen Loaded Microspheres of Cellulosic and Polymethacrylic Polymeric Blend." Dhaka University Journal of Pharmaceutical Sciences 12, no. 1 (2013): 11–21. http://dx.doi.org/10.3329/dujps.v12i1.16295.

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Naproxen, a well-known non-steroidal anti-inflammatory drug was encapsulated with cellulosic and polymethacrylic polymers to provide sustained action and to minimize gastro esophageal side effects by avoiding the release of drug in the upper gastrointestinal tract. Emulsification-solvent evaporation technique using Ethyl Cellulose, Eudragit RSPO and their combination as release retardant was the method of choice. The formulations were prepared by keeping the amount of drug fixed to 1g and the total amount of polymer fixed to 1g in which Ethyl Cellulose and Eudragit RSPO were used in varying co

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7

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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8

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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9

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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10

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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