Relevant bibliographies by topics / Enteric-coated tablets. Drugs

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  1. Journal articles
  2. Dissertations / Theses
  3. Conference papers

Academic literature on the topic 'Enteric-coated tablets. Drugs'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "Enteric-coated tablets. Drugs"

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Peters, I. O. M., A. Willemsen, J. J. de Bruyne, and R. C. Nap. "Aspirin Medication in Dogs." Veterinary and Comparative Orthopaedics and Traumatology 4, no. 03 (1991): 95–99. http://dx.doi.org/10.1055/s-0038-1633260.

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SummaryAspirin (acetylsalicylic acid; ASA) is widely used in both human and veterinary medicine. Therapeutic plasma salicylate concentrations (PSCs) can be reached using enteric-coated ASA tablets, but a delay in the initial rise and large fluctuations in the PSCs have been reported. From experiments described previously, the authors concluded that the large type enteric-coated ASA tablets were not suitable for use in beagle dogs.In the first experiment described here, these large type tablets were administered to large mongrel dogs. Although the mean PSC reached therapeutic levels after 44 h,
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Patel, Hetal, and Mukesh Gohel. "A Review on Enteric Coated Pellets Composed of Core Pellets Prepared by Extrusion-Spheronization." Recent Patents on Drug Delivery & Formulation 13, no. 2 (2019): 83–90. http://dx.doi.org/10.2174/1872211313666190212115139.

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Enteric coated dosage form bypasses the stomach and releases the drug into the small intestine. Advantages of enteric coated pellets in comparison with enteric coated tablets are a) Pellets provide rapid onset of action and faster drug release due to the smaller size than tablets and b) Pellets exhibit less residence time of acid-labile drugs in the stomach compared to tablets. Dosage form coat can be damaged by longer resistance time in the stomach. The present review summarizes the current state of enteric coated pellets where core pellets are prepared by extrusion-spheronization technique a
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Godge, GR, and SN Hiremath. "Development and evaluation of colon targeted drug delivery system by using natural Polysaccharides/Polymers." Dhaka University Journal of Pharmaceutical Sciences 13, no. 1 (2015): 105–13. http://dx.doi.org/10.3329/dujps.v13i1.21874.

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Colon is being extensively investigated as a drug delivery site. This study contains comparison of the usual enteric coating polymers viz. xanthan gum, guar gum, chitosan and ethyl cellulose, as carriers for colon specific drug delivery. Lactose based metoprolol succinate tablets were prepared. These were coated with one of the coating polymers to a varying coat thickness. Tablets were prepared using polysaccharides or synthetic polymer as binders. These included xanthan gum, guar gum, chitosan and ethyl cellulose. Metoprolol Succinate was used as a model drug. The prepared tablets were enteri
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Parys, Wioletta, Alina Pyka-Pająk, and Małgorzata Dołowy. "Application of Thin-Layer Chromatography in Combination with Densitometry for the Determination of Diclofenac in Enteric Coated Tablets." Pharmaceuticals 12, no. 4 (2019): 183. http://dx.doi.org/10.3390/ph12040183.

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Diclofenac belongs to the drug class non-steroidal anti-inflammatory drugs widely used in Europe as well as all over the world. Thus, it is important to conduct research on its quality control of available pharmaceutical preparations like for example enteric coated tablets. Among various analytical techniques, thin-layer chromatography (TLC) is ideal for this task due to their short time analysis, ease of operation and low cost. Hence, the aim of this study was to develop the optimal conditions of analysis and quantitative determination of diclofenac sodium in enteric tablets by using TLC in c
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Doye, Pakpi, Tanya Mena, and Nilimanka Das. "FORMULATION AND BIO-AVAILABILITY PARAMETERS OF PHARMACEUTICAL SUSPENSION." International Journal of Current Pharmaceutical Research 9, no. 3 (2017): 8. http://dx.doi.org/10.22159/ijcpr.2017.v9i3.18892.

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The suspension is a biphasic liquid or semi-solid dosage form where the finely divided insoluble solid drug particles are homogeneously dispersed in a liquid or semi-solid medium. The solid drug particles act here as the dispersed phase and the liquid or the semi-solid as the dispersion medium. Suspensions contribute to pharmaceutical dosage form development by supplying drugs that are insoluble in all acceptable medium and often distasteful. Suspension translates such drugs into more bio-available form when compared to capsules, tablets, coated tablets, enteric coated tablets and sustained re
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Nykänen, P., S. Lempää, M. L. Aaltonen, H. Jürjenson, P. Veski, and M. Marvola. "Citric acid as excipient in multiple-unit enteric-coated tablets for targeting drugs on the colon." International Journal of Pharmaceutics 229, no. 1-2 (2001): 155–62. http://dx.doi.org/10.1016/s0378-5173(01)00839-0.

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Induja, L., Aslam T. A., and G. Andhuvan. "PHARMACIST INTERVENTION AND PREPARATION OF MANUAL IN THE ADMINISTRATION OF DRUGS THROUGH ENTERAL FEEDING TUBE." International Journal of Pharmacy and Pharmaceutical Sciences 10, no. 12 (2018): 21. http://dx.doi.org/10.22159/ijpps.2018v10i12.27655.

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Objective: To monitor errors in current practice and prepare a manual for proper drug administration through the enteral feeding tube.Methods: It is a prospective observational study conducted for a period of 6 mo in eight departments. The current drug administrations were monitored and checked for the errors which include crushed non crushable solid dosage forms, each drug is not prepared separately, incorrect solution used for dilution, drugs mixed with feeding formula, each drug is not administered separately, not flushed before administration of each drug, not flushed after administration
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Xiong, Zhencheng, Ping Yi, Liubo Zhang, Haoning Ma, Wenhao Li, and Mingsheng Tan. "Efficacy and Safety of Modified Duhuo Jisheng Decoction in the Treatment of Lumbar Disc Herniation: A Systematic Review and Meta-Analysis." Evidence-Based Complementary and Alternative Medicine 2020 (July 4, 2020): 1–11. http://dx.doi.org/10.1155/2020/2381462.

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Objective. Lumbar disc herniation (LDH) is based on the degenerative changes of the intervertebral disc. Many drugs are used to treat and prevent LDH, including Western medicine and Chinese medicine. Duhuo Jisheng Decoction (DHJSD) is one of the most classic Chinese medicine prescriptions. The purpose of our meta-analysis is to evaluate the efficacy and safety of modified DHJSD in the treatment of LDH. Methods. We searched multiple databases including PubMed, Embase, Cochrane Library, China National Knowledge Infrastructure (CNKI) databases, Wanfang Database, and Chinese Scientific Journal Dat
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Pereira, Rosana Aparecida, Fabiana Bolela de Souza, Mayara Carvalho Godinho Rigobello, José Rafael Pereira, Laís Rosa Moreno da Costa, and Fernanda Raphael Escobar Gimenes. "Quality improvement programme reduces errors in oral medication preparation and administration through feeding tubes." BMJ Open Quality 9, no. 1 (2020): e000882. http://dx.doi.org/10.1136/bmjoq-2019-000882.

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BackgroundPatients with nasogastric/nasoenteric tube (NGT/NET) are at increased risk of adverse outcomes due to errors occurring during oral medication preparation and administration.AimTo implement a quality improvement programme to reduce the proportion of errors in oral medication preparation and administration through NGT/NET in adult patients.MethodsAn observational study was carried out, comparing outcome measures before and after implementation of the integrated quality programme to improve oral medication preparation and administration through NGT/NET. A collaborative approach based on
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Genç, Lütfi, Erden Güler, and Nahed Hegazy. "Film-Coated Enteric Tablet Formulation of Ketorolac Tromethamine." Drug Development and Industrial Pharmacy 23, no. 10 (1997): 1007–11. http://dx.doi.org/10.3109/03639049709149154.

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Dissertations / Theses on the topic "Enteric-coated tablets. Drugs"

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Murty, Aruna Mummini. "Evaluation of potential multi-particulate drug delivery systems /." View online ; access limited to URI, 2006. http://0-wwwlib.umi.com.helin.uri.edu/dissertations/dlnow/3225324.

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Sauer, Dorothea 1979. "An investigation of formulation factors and processing parameters for the powder-coating of tablets." Thesis, 2008. http://hdl.handle.net/2152/3942.

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Dry powder coating of pharmaceutical dosage forms has been investigated as an alternative method to commonly used liquid based coating techniques. Eudragit[trademark] L 100-55 and Eudragit[trademark] L 30 D-55 have been employed in enteric film coatings using aqueous dispersions, organic solutions and compression coating. However, the copolymer has not been investigated in dry powder coating applications. Initially, formulation factors and processing parameters were investigated for the dry powder coating of chlorpheniramine maleate tablets using Eudragit[trademark] L 100-55 as the delayed r
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Cook, Rebecca. "In-vitro testing of the influence of ethanol on the release rate of oral extended-release solid dosage forms." 2007. http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.13454.

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Leung, Manshiu. "Tablet shapes and in vitro evaluation of coated hydrophilic matrix tablets novel mupirocin formulations non-acidic enteric coating of omeprazole and novel hot-melt coating process." Thesis, 2002. http://hdl.handle.net/1957/31105.

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This dissertation is comprised of four distinct formulation sections, which are described below: A novel solid dosage formulation was investigated for achieving zero-order drug release profile by combining tablet shape design and tablet membrane film coating. Verapmail (model drug) was compressed into hydrophilic matrix tablet cores of flat-faced and bi-convex shape, which were encapsulated with membrane controlling film. The hydrophilic tablet core contained hydroxypropyl methylcellulose (HPMC) 15 LV, pectin, and Avecil��. The membrane film coating solution was comprised of deionized water, O
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Watanalumlerd, Prapoch. "1) Pharmacokinetic modeling and simulations of gastrointestinal transit effects on drug pharmacokinetics from enteric-coated pellet formulations and their applications ; 2) development of crushable enteric-coated formulations ; 3) development of leaky enteric-coated pellets formulations." Thesis, 2004. http://hdl.handle.net/1957/28850.

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Effects of gastrointestinal transit on plasma concentrations of drugs from enteric-coated pellet formulations were demonstrated using pharmacokinetic models describing plasma concentrations of drugs from various enteric-coated pellet formulations. Gastric emptying time, lag time of emptying, and drug release rate from pellets in the small intestine, along with other pharmacokinetic parameters of drugs, were used to construct pharmacokinetic models. The models were then evaluated by comparing simulated plasma concentrations of model drugs from Monte Carlo simulations to observed plasma concentr
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Tantituvanont, Angkana. "Novel formulation : development of oral microparticulate non-viral DNA vaccine delivery system against infectious hematopoetic necrosis virus (IHNV) in Rainbow Trout, statistical design in matrix tablets formulation." Thesis, 2003. http://hdl.handle.net/1957/31818.

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This dissertation describes two different projects. The first is the development of an oral DNA vaccine delivery system for fish. A novel oral DNA vaccine delivery system was developed for Rainbow Trout by combining non-viral vectors (polycationic liposomes or polycationic polymer) to facilitate the DNA vaccine's uptake by cell membranes along with enteric-coated protection of the DNA embedded in microparticles to prevent DNA degradation in the gastrointestinal tract. Spray drying and spray coating bead techniques were employed in the preparation of the DNA vaccine microparticles. The spray dr
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Conference papers on the topic "Enteric-coated tablets. Drugs"

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Venkatakrishnan, Karthik, Jeffrey R. Infante, Roger B. Cohen, et al. "Abstract C122: Phase 1b relative bioavailability (BA) study of enteric coated tablet (ECT) in reference to powder in capsule (PIC) formulation of the investigational drug alisertib (MLN8237), an Aurora A Kinase (AAK) inhibitor, in patients with advanced nonhematologic malignancies." In Abstracts: AACR-NCI-EORTC International Conference: Molecular Targets and Cancer Therapeutics--Nov 12-16, 2011; San Francisco, CA. American Association for Cancer Research, 2011. http://dx.doi.org/10.1158/1535-7163.targ-11-c122.

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