Academic literature on the topic 'KollicoatIR'

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Journal articles on the topic "KollicoatIR"

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SK., Shahanaj* Sasikanth Kothamasu Manohar Babu S. "FORMULATION DEVELOPMENT AND EVALUATION OF FAST RELEASE FILMS OF GALANTAMINE." Indo American Journal of Pharmaceutical Sciences 04, no. 07 (2017): 2164–69. https://doi.org/10.5281/zenodo.837294.

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In the present work efforts have been made to prepare the fast dissolving films of Galantamine using water soluble semi synthetic polymers such as HPMC 3cps, Na CMC and KollicoatIR using plasticizer by means of sodium starch glycolate, super-disintegrants by using the solvent casting method. By comparing with the marketed tablet, the FDFs formulated by means of using superdisintegrant showed fast release for quicker onset of action within minutes. The prepared films were evaluated for physico-chemical properties and invitro release kinetics. The selected formulations produced clear, uniform, f
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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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Komanduri, Neeraja, Mashan Almutairi, Rasha M. Elkanayati, et al. "Kollicoat® Smartseal 100P for Developing Theophylline Pellets: Exploring Taste-Masking Potential for Pediatric Applications." Pharmaceutics 17, no. 4 (2025): 413. https://doi.org/10.3390/pharmaceutics17040413.

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Background/Objectives: This study aimed to develop and evaluate taste-masked theophylline pellets using hot-melt extrusion (HME) technology. Additionally, the study evaluates the efficacy of various taste-masking polymers by comparing three pH-dependent polymers, Kollicoat® Smartseal 100P, Eudragit® EPO, and Kollicoat® MAE 100-55, in masking taste and optimizing drug release. Methods: Formulations were designed with varying drug loads (10%, 20%, and 30%) and plasticizer concentrations (20% and 30% PEG 1500). Lead formulations were characterized using differential scanning calorimetry (DSC), Fo
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Fouad, Ehab A., Mahmoud El-Badry, Steven H. Neau, Fars K. Alanazi, and Ibrahim A. Alsarra. "Technology evaluation: Kollicoat IR." Expert Opinion on Drug Delivery 8, no. 5 (2011): 693–703. http://dx.doi.org/10.1517/17425247.2011.566266.

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Luke, Stefani, Martha Ervina, and Lannie Hadisoewignyo. "Optimization of Coating Formula of White Pomegranate Peel Extract (Punica granatum L.) Film Coated Tablet Using Kollicoat Protect." Indonesian Journal of Pharmaceutical Research 1, no. 1 (2021): 19–27. http://dx.doi.org/10.31869/ijpr.v1i1.1993.

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White pomegranate peel has many kinds uses, one of them as antimalaria. The unpleasant appearance and bitter taste of white pomegranate peel tablet can be covered by film coated using Kollicoat Protect. This research aimed to determine the effect of concentration and type of solvent used as a coating on the physical properties of the coated tablets and determine the optimum formula. Tablets were made using direct compression method and then coated using Kollicoat Protect. The optimization of coating formula was performed using a factorial design with design expert software ver 10.0. Responses
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Rahman, Tanvir, Md Abdurrahim, Koma Afrin Rintu, et al. "Improvement of in vitro dissolution profile of poorly aqueous soluble anti-parasitic agent ivermectin using novel hydrophilic polymeric carriers." Bangladesh Journal of Scientific and Industrial Research 58, no. 4 (2023): 209–20. http://dx.doi.org/10.3329/bjsir.v58i4.69047.

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Ivermectin (IVM), a BCS Class II drug with weak water solubility, has minimal oral absorption and dissolution. This study aims to enhance the dissolution profile of IVM by performing solid dispersion methods using four hydrophilic polymers: Kollicoat IR, Kollidon 90F, poloxamer 407, and hydroxypropyl methylcellulose (HPMC). The solid dispersion formulations (SDF) were made through physical mixing, solvent evaporation, and melt solvent/fusion. Using three ratios of IVM and hydrophilic carriers (1:1, 1:2, and 1:3), the cumulative release rate of IVM from formulations formed by physical mixing, s
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Xi, Ziyue, Wei Zhang, Yali Fei, et al. "Evaluation of the Solid Dispersion System Engineered from Mesoporous Silica and Polymers for the Poorly Water Soluble Drug Indomethacin: In Vitro and In Vivo." Pharmaceutics 12, no. 2 (2020): 144. http://dx.doi.org/10.3390/pharmaceutics12020144.

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This work explored absorption efficacy via an in vivo imaging system and parallel artificial membrane penetration in indomethacin (IMC) solid dispersion (SD) systems. Two different polymer excipients—hydroxypropyl methylcellulose (HPMC) and Kollicoat IR as precipitation inhibitors (PIs)—combined with mesoporous silica nanoparticles (MSNs) as carriers were investigated. The IMC–SDs were prepared using the solvent evaporation method and characterized by solubility analysis, infrared (IR) spectroscopy, powder X-ray diffraction (PXRD), field emission scanning electron microscopy (FESEM), and diffe
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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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Fahier, Julie, Branko Vukosavljevic, Laure De Kinder, et al. "Towards a Better Understanding of Verapamil Release from Kollicoat SR:IR Coated Pellets Using Non-Invasive Analytical Tools." Pharmaceutics 13, no. 10 (2021): 1723. http://dx.doi.org/10.3390/pharmaceutics13101723.

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The aim of this study was to gain deeper insight into the mass transport mechanisms controlling drug release from polymer-coated pellets using non-invasive analytical tools. Pellet starter cores loaded with verapamil HCl (10% loading, 45% lactose, 45% microcrystalline cellulose) were prepared by extrusion/spheronization and coated with 5% Kollicoat SR:IR 95:5 or 10% Kollicoat SR:IR 90:10. Drug release was measured from ensembles of pellets as well as from single pellets upon exposure to acetate buffer pH = 3.5 and phosphate buffer pH = 7.4. The swelling of single pellets was observed by optica
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Maraie, Nidhal K., Zeina D. Salman, and Nora Zawar Yousif. "DESIGN AND CHARACTERIZATION OF OROSLIPPERY BUOYANT TABLETS FOR RANITIDINE HYDROCHLORIDE." Asian Journal of Pharmaceutical and Clinical Research 11, no. 1 (2018): 143. http://dx.doi.org/10.22159/ajpcr.2017.v11i1.21982.

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Objective: The goal behind of performing this study was to come out with an oroslippery buoyant ranitidine hydrochloride tablet to ease the swallowing process. Hence, the drug is released controllably in the stomach regardless of the effect on gastric emptying time.Materials and Methods: The core of the buoyant containing 150 mg of the drug was compressed directly, and sodium bicarbonate was employed as an effervescent agent, besides, hydroxyl propyl methyl cellulose (HPMC) polymer was utilized in different grades in the formulation process. The prepared core was immersed in the coating disper
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Dissertations / Theses on the topic "KollicoatIR"

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Zanin, Giovane Douglas. "Influência do ácido hialurônico na formação de filmes isolados de acetato polivinílico destinados ao revestimento de sólidos orais." Universidade Estadual do Oeste do Paraná, 2014. http://tede.unioeste.br/handle/tede/3487.

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Submitted by Neusa Fagundes (neusa.fagundes@unioeste.br) on 2018-03-06T19:28:50Z No. of bitstreams: 2 Giovane_Zanin2014.pdf: 3169659 bytes, checksum: ca4852dea2558da8d3c74260c79fc413 (MD5) license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5)<br>Made available in DSpace on 2018-03-06T19:28:50Z (GMT). No. of bitstreams: 2 Giovane_Zanin2014.pdf: 3169659 bytes, checksum: ca4852dea2558da8d3c74260c79fc413 (MD5) license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5) Previous issue date: 2014-09-26<br>Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAP
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Pezzini, Bianca Ramos. "Dissolução de comprimidos e péletes de liberação prolongada empregando-se os métodos da pá e Bio-Dis." Universidade de São Paulo, 2007. http://www.teses.usp.br/teses/disponiveis/9/9139/tde-17072017-100425/.

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Matrizes hidrofílicas de diclofenaco sódico e de cetoprofeno foram preparadas por meio de compressão direta ou granulação úmida seguida de compressão, utilizando-se hipromelose para modular a dissolução do fármaco. Foram também obtidos péletes de liberação prolongada de cetoprofeno, mediante extrusão-esferonização e revestimento, em leito fluidizado, com Kollicoat® EMM 30D. Um planejamento fatorial 22 foi usado para elucidar os efeitos de variáveis de formulação sobre os perfis de liberação do fármaco a partir dos sistemas em estudo, determinados empregando-se os métodos da pá e/ou Bio-Dis. No
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Book chapters on the topic "KollicoatIR"

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Cech, Thorsten, and Jan-Peter Mittwollen. "Coating mit Kollicoat®." In Easy Coating. Vieweg+Teubner, 2011. http://dx.doi.org/10.1007/978-3-8348-9896-8_6.

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