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Journal articles on the topic 'Kollicoat SR'

Author: Grafiati
Published: 3 June 2025
Last updated: 31 July 2025

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1

V., Madhu Sudarsan* S.T.V. Raghavamma N. Rama Rao. "FORMULATION AND EVALUATION OF METOPROLOL SUCCINATE EXTENDED RELEASE TABLETS COMPRISING COATED PELLETS." INDO AMERICAN JOURNAL OF PHARMACEUTICAL SCIENCES o6, no. 08 (2019): 14659–74. https://doi.org/10.5281/zenodo.3368085.

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<em>The objective of the present study was for improving bioavailability and reducing the dosage frequency of Metoprolol succinate in the form of extended release pellets by pan coating technology.</em><em> Preliminary studies with different polymers such as Surelase, Ethyl cellulose N50, Kollicoat SR 30D were performed. The results of in-vitro release data showed that Kollicoat SR 30D can Extend the drug release up to 24hr. Metoprolol succinate extended release tablets were prepared by MUPS Technique. The hardness of these extended release tablets was within the limit. The drug content was wi
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2

P.Eswaramma*, M.Vijaya kumari G.Sruthi V.Yamini Saraswathi A. Naveen Kumar G. Rajasekhar M. Raja Rathnam. "FORMULATION AND EVALUATION OF EXTENDED RELEASE PELLETS OF METOPROLOL SUCCINATE." Indo American Journal of Pharmaceutical Sciences 04, no. 08 (2017): 2308–20. https://doi.org/10.5281/zenodo.843647.

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The objective of the present study was to formulate and develop extended release drug delivery system of antihypertensive drug Metoprolol succinate . The major indications of Metoprolol succinate is treatment and management of hypertension, angina, acute myocardial infarction, supraventricular tachycardia, congestive heart faiure, and migrane. Hypertension (HTN)is a chronic medical condition in which the blood pressure in the arteries is elevated. High blood pressure is said to be present if it is persistently at or above 140/90 mmHg pressure . The dosage for adults is 2-3 times a day, to redu
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3

Li-Fang, Fan, He Wei, Chang Yong-Zhen, et al. "Studies of chitosan/Kollicoat SR 30D film-coated tablets for colonic drug delivery." International Journal of Pharmaceutics 375, no. 1-2 (2009): 8–15. http://dx.doi.org/10.1016/j.ijpharm.2009.03.023.

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4

Wei, He, Fan Li-Fang, Bai Min, et al. "Chitosan/Kollicoat SR 30D film-coated pellets of aminosalicylates for colonic drug delivery." Journal of Pharmaceutical Sciences 99, no. 1 (2010): 186–95. http://dx.doi.org/10.1002/jps.21810.

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5

Sawicki, Wiesław, and Rafał Łunio. "Compressibility of floating pellets with verapamil hydrochloride coated with dispersion Kollicoat SR 30 D." European Journal of Pharmaceutics and Biopharmaceutics 60, no. 1 (2005): 153–58. http://dx.doi.org/10.1016/j.ejpb.2004.11.003.

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6

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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7

Andreazza, Itamar Francisco, and Humberto Gomes Ferraz. "Preparation of pellets containing highly soluble drug by extrusion/spheronisation and coating with Kollicoat® SR 30D." Brazilian Archives of Biology and Technology 54, no. 2 (2011): 315–20. http://dx.doi.org/10.1590/s1516-89132011000200013.

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8

Cho, Hyuk Jun, Jung Suk Kim, Sung Giu Jin, and Han-Gon Choi. "Development of Novel Tamsulosin Pellet-Loaded Oral Disintegrating Tablet Bioequivalent to Commercial Capsule in Beagle Dogs Using Microcrystalline Cellulose and Mannitol." International Journal of Molecular Sciences 24, no. 20 (2023): 15393. http://dx.doi.org/10.3390/ijms242015393.

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In this study, we developed a tamsulosin pellet-loaded orally disintegrating tablet (ODT) that is bioequivalent to commercially available products and has improved patient compliance using microcrystalline cellulose (MCC) and mannitol. Utilizing the fluid bed technique, the drug, sustained release (SR) layer, and enteric layer were sequentially prepared by coating MCC pellets with the drug, HPMC, Kollicoat, and a mixture of Eudragit L and Eudragit NE, respectively, resulting in the production of tamsulosin pellets. The tamsulosin pellet, composed of the MCC pellet, drug layer, SR layer, and en
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9

Shao, Zezhi J., Luis Morales, Steven Diaz, and Nouman A. Muhammad. "Drug release from kollicoat SR 30D-coated nonpareil beads: Evaluation of coating level, plasticizer type, and curing condition." AAPS PharmSciTech 3, no. 2 (2002): 87–96. http://dx.doi.org/10.1208/pt030215.

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10

Dashevsky, A., K. Kolter, and R. Bodmeier. "pH-independent release of a basic drug from pellets coated with the extended release polymer dispersion Kollicoat® SR 30 D and the enteric polymer dispersion Kollicoat® MAE 30 DP." European Journal of Pharmaceutics and Biopharmaceutics 58, no. 1 (2004): 45–49. http://dx.doi.org/10.1016/j.ejpb.2004.03.013.

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11

Dashevsky, A., K. Wagner, K. Kolter, and R. Bodmeier. "Physicochemical and release properties of pellets coated with Kollicoat® SR 30 D, a new aqueous polyvinyl acetate dispersion for extended release." International Journal of Pharmaceutics 290, no. 1-2 (2005): 15–23. http://dx.doi.org/10.1016/j.ijpharm.2004.10.024.

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12

Elkordy, Amal Ali, Xin Ning Tan, and Ebtessam Ahmed Essa. "Spironolactone release from liquisolid formulations prepared with Capryol™ 90, Solutol® HS-15 and Kollicoat® SR 30 D as non-volatile liquid vehicles." European Journal of Pharmaceutics and Biopharmaceutics 83, no. 2 (2013): 203–23. http://dx.doi.org/10.1016/j.ejpb.2012.08.004.

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13

Mohammed, Mushtaq J., and Wedad K. Ali. "Formulation and In-vitro Evaluation of Two Layers Tablet for Dual Release of a Model Drug." INTERNATIONAL JOURNAL OF DRUG DELIVERY TECHNOLOGY 13, no. 01 (2023): 45–56. http://dx.doi.org/10.25258/ijddt.13.1.08.

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Objective: Glimepiride is a third-generation sulfonylurea medication that has been used to treat type 2 diabetes (T2D) mellitus. It is class II drug according to the biopharmaceutical classifi cation system (BCS) characterized with its low solubility and high permeability. Due to the drug’s weak water solubility, its bioavailability is restricted by its dissolving rate. This study aimed to develop a bilayer tablet of glimepiride with one layer for immediate release (IR), a dose of 2 mg, a second layer for sustained release (SR), and a 4 mg dose Immediate release layer included solid dispersion
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14

Rathi, Sanjesh G., Shrenik K. Shah, Sohansinh S, and Himanshu G. Parmar. "Formulation and Evaluation of Delayed Release Pellets of Ivabradine Hydrochloride." International Journal of Pharmaceutical Sciences Review and Research 69, no. 1 (2021). http://dx.doi.org/10.47583/ijpsrr.2021.v69i01.029.

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The aim of preset research work is to formulate and evaluate delayed release pellets of Ivabradine HCl. Pellets are prepared using extrusion-spheronization process and the process parameters are optimized. Polymer coating done with Kollicoat SR 30 D as rate controlling polymer and finally enteric coating done with Eudragit L30D-55. Drug release in formulation F1-F9 studied and it found that the low polymer concentration (2 %) was unable to retard the drug release up to 12 hr so concentration increased batch by batch and finally 12 % coating batch gives desired results which retard the drug rel
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15

Yadav, Vishal, and S. Sathesh Kumar Yadav. "Formulation and Evaluation of Extended Release Capecitabine Loaded Pellets." International Journal of Drug Delivery Technology 9, no. 02 (2019). http://dx.doi.org/10.25258/ijddt.9.2.8.

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Capecitabine is a well known orally-administered anticancer agent utilized in the treatment of colorectal cancer and metastatic breast cancer. The present study reveals the development and evaluation of an extended release Capecitabine loaded pellets. The Capecitabine loaded pellets were prepared by using a layering process followed by Wurster Process and made it extended release using Ethylcellulose (EC), Polyvinyl Pyrrolidone (PVP-K30) and Kollicoat SR 30D coating. The prepared extended release pellets were characterized by FTIR, SEM, DSC and XRD studies. The extended-release pellets also ev
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