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Dissertations / Theses on the topic 'Enteric Coated'

Author: Grafiati

Published: 2 June 2025

Last updated: 31 July 2025

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1

Fu, Maoqi [Verfasser]. "Enteric-coated HPMC capsules: Comparison of enteric coatings and investigation of relationship between in-vitro disintegration and dissolution times / Maoqi Fu." Mainz : Universitätsbibliothek Mainz, 2020. http://d-nb.info/1213058619/34.

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2

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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3

LALWANI, DARSHAN NARENDRA. "An oral dosage form of ceftriaxone sodium using enteric coated sustained release calcium alginate beads." University of Toledo Health Science Campus / OhioLINK, 2015. http://rave.ohiolink.edu/etdc/view?acc_num=mco1430403186.

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4

Wu, Chuanbin. "Influence of non-traditional plasticizers and enteric polymers on the physicochemical and mechanical properties of polymeric films and film coated solid substrates /." Digital version accessible at:, 1999. http://wwwlib.umi.com/cr/utexas/main.

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5

Niestadtkötter, Gerd-Jonas [Verfasser], Lutz Peter [Gutachter] Müller, Gerald [Gutachter] Wulf, and Philipp [Gutachter] Hemmati. "Akute Graft versus Host Erkrankung und gastrointestinale Toxizität nach allogener Stammzelltransplantation bei der Prophylaxe mit Enteric-coated mycophenolate sodium, Methotrexat und Mycophenolat-mofetil / Gerd-Jonas Niestadtkötter ; Gutachter: Lutz Peter Müller, Gerald Wulf, Philipp Hemmati." Halle (Saale) : Universitäts- und Landesbibliothek Sachsen-Anhalt, 2020. http://d-nb.info/1212031660/34.

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6

Heischmann, Svenja [Verfasser], Uwe [Akademischer Betreuer] Christians, Dieter [Akademischer Betreuer] Leibfritz, and Wolf-Dieter [Akademischer Betreuer] Stohrer. "Identification of the Molecular Mechanisms underlying the Gastrointestinal Toxicity of the Immunosuppressants Mycophenolate Mofetil and Enteric-coated Mycophenolate Sodium using a Proteo-Metabolomic Approach / Svenja Heischmann. Gutachter: Dieter Leibfritz ; Wolf-Dieter Stohrer. Betreuer: Uwe Christians." Bremen : Staats- und Universitätsbibliothek Bremen, 2013. http://d-nb.info/1072156245/34.

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7

Siebert, Barbara Stephanie [Verfasser], Stefan G. [Akademischer Betreuer] Thorban, Helmut [Akademischer Betreuer] Friess, and Jörg H. [Akademischer Betreuer] Kleeff. "Enteric-coated Mycophenolsäure (EC-MPA) in der Nierentransplantation - Nutzen der IMPDH-Enzymaktivitätsmessung sowie Evaluation der Nebenwirkungen hinsichtlich der Lebenszufriedenheit / Barbara Stephanie Siebert. Gutachter: Helmut Friess ; Stefan G. Thorban ; Jörg H. Kleeff. Betreuer: Stefan G. Thorban." München : Universitätsbibliothek der TU München, 2013. http://d-nb.info/1037430778/34.

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8

Mudau, Muvhulawa Sylvia. "Functional properties of microwave pasteurised and oil coated whole shell eggs." Diss., University of Pretoria, 2007. http://hdl.handle.net/2263/26837.

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Food borne infections due to Salmonella enterica serovar Enteritidis (S. Enteritidis) has shown a dramatic increase in many countries. Different egg pasteurisation treaments have been developed in the past but are still not providing practical or optimal solutions. A method is required that ensure that eggs are microbiologically safe, that does not affect the functional quality and possibly also extend the egg shelf life. This research project formed part of a larger study, “Project 32438: The development of a novel microwave system for the pasteurisation of raw whole shell eggs” funded by the

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9

Rodsand, Pouria. "Uptake of super paramagnetic iron oxide by astrocytes : The ability of super paramagnetic iron oxide nanoparticles coated with L-DOPA to enter astrocytes in vitro." Thesis, Umeå universitet, Kemiska institutionen, 2014. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-85838.

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10

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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11

Wong, George Kaon. "Development of novel oral enteric-coated aquaculture vibrio vaccines." Thesis, 1990. http://hdl.handle.net/1957/37467.

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An oral Vibrio vaccine for salmonids was developed. The vaccine was produced by spray coating lyophilized formalin-killed whole cells of Vibrio anguillarum (VA LS 1- 74) onto non-pareil sugar beads. Then methacrylic acrylic acid copolymer (Eudragit L-30D) was applied as an enteric protective coating. Using x-ray radiographic techniques, it was found that large particles (> 1.1 mm) remain in the fish stomach for more than 2 hours before they would enter the pyloric caeca. The pyloric sphincter which has an opening of 0.94 mm, acts as barrier to prevent the passage of large food particles in the

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12

Hsiao, Li-Chung, and 蕭力中. "Study On Enteric Coating Layer Formulation And Coating Process Of Doxycycline Hydrochloride Enteric Coated Pellets." Thesis, 2018. http://ndltd.ncl.edu.tw/handle/m434y2.

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碩士<br>中國醫藥大學<br>製藥碩士學位學程<br>106<br>Coat hydrochloric acid doxycycline enteric-coated pellets with different dissolution characteristics enteric coating, HPMC-P and EUDRAGIT® L30D-55, in different coating process; identify their dissolution, roundness, and friability in 0.06M HCl solution and pH 5.5 buffer solution as well as impact of intense light, high temperature and high humidity on the product and its accelerated stability. Initial results suggest HPMC-P and EUDRAGIT® L30D-55 based products make no significant difference in acid and pH5.5 buffer solution in terms of dissolution. Particles

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13

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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14

Lin, Sue-Feng, and 林素鳳. "Preparation and in vitro evaluation of lansoprazole enteric coated pellets." Thesis, 2004. http://ndltd.ncl.edu.tw/handle/17901221789958110891.

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碩士<br>高雄醫學大學<br>藥學研究所碩士班<br>92<br>Lansoprazole is an effective proton pump inhibitor, but it is a poor- solubility drug. Inclusion complexes between lansoprazole and hydroxyl- propyl- β- cyclodextrin ( HPβCD ) were prepared to improve the solubility of lansoprazole and evaluated in aqueous environment and in solid state. From the phase solubility study results, lansoprazole showed AL type phase solubility in pH 8 and pH 10 medium, demonstrating the formation of 1: 1 stoichiometric inclusion complexes. Lansoprazole showed BS type phase solubility in pH 12 medium, and the decreasing of solubili

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15

Lee, Chu-Huei, and 李燭惠. "The influence of antacid on bioavailability of enteric-coated aspirin granules." Thesis, 2000. http://ndltd.ncl.edu.tw/handle/14843812208241019644.

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碩士<br>高雄醫學大學<br>藥學研究所<br>88<br>Aspirin capsules contain 100 mg enteric-coated granules. These enteric-coated granules are delayed-released to avoid aspirin-induced gastric irritation. Antacids neutralize gastric acid and increase pH. After coadministration of enteric-coated aspirin granules and antacids, aspirin may be dissoluted in the stomach, not in the intestine, and lose the delayed-released characteristics. This study contained four parts: first, retrospective review of prescription with enteric-coated aspirin granules. second, the influence of antacids on the pH value of dis

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16

Chen, Shih-Kai, and 陳世凱. "The Development of Formula and Quality Control Method for Enteric Coated Hard Capsules." Thesis, 2006. http://ndltd.ncl.edu.tw/handle/98716981824240477054.

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碩士<br>朝陽科技大學<br>應用化學系碩士班<br>94<br>This research uses one kind of hydroxy propyl methylcellulose (Hypromellose Acetate Succinate, AS-LF) as the superposition colloid of the enteric coated hard capsules. Formula proportion：ethyl alcohol 76%, methylene chloride 11%, and AS-LF powder 13%. The hard capsules were moistened in formula solution at the temperature approximately 33℃. Then dry approximately 5 minutes at 35 ℃ following cold wind for about 10 minutes. The superposition colloid prepared by this partition controls temperature dryness process, can form am egual thickness membrane on the capsu

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17

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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18

Knöll, Marcus Hans [Verfasser]. "Enteric coated mucoadhesive micropellets in rotary agglomeration process for wet spheronization / Marcus Hans Knöll." 2007. http://d-nb.info/982846665/34.

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19

ZHAN, YI-LIANG, and 詹益亮. "Study on microencapsulation of enteric-coated mycoplasma hyopneumoniae oral vaccine and its medication efficacy." Thesis, 1991. http://ndltd.ncl.edu.tw/handle/63574679411123725155.

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20

Wang, Ya-Hsien, and 王雅嫻. "The Development of Formula and Quality Control Method for Aspirin Enteric-coated Hard Capsules." Thesis, 2007. http://ndltd.ncl.edu.tw/handle/89200082288366449411.

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碩士<br>朝陽科技大學<br>應用化學系碩士班<br>95<br>This research uses hydroxypropyl methylcellulose acetate succinate﹙HPMCAS﹚ to made the intestine dissolved colloid as the coating material of the hard capsule. The purpose of this coating is using its characteristic to prevent the aspirin capsule breaking up in the stomach, until the capsule migrate to intestine and breaks up to the drug. The aspirin would not to injure the stomach by this way. The research including the discussion of the intestine dissolved colloid formula, the disintegration test and, the dissolution test of capsules, as well as the stabilit

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21

Horng, Lin Jiunn, and 林俊宏. "The Application of Co-Spray Drying Technology to Enteric-Coated Microspheres Oral Vaccine for Animal Use." Thesis, 2003. http://ndltd.ncl.edu.tw/handle/31287381451481298161.

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博士<br>國立臺灣大學<br>獸醫學研究所<br>91<br>In this study, M. hyopneumoniae was used as core materials and Eudragit L30 D55 or Aquacoat ECD was used as a coating material to produce microspheres by co-spray drying process. The characterization of microspheres was evaluated with physicochemical methods in vitro and immunogenicity of the entrapped antigen was determinate in vivo. Adjuvant was also added to microspheres vaccine for increasing the efficiency of vaccination. In vitro study revealed that the optimum storage temperature was 4°C. The storage time for T1E15 is one month, while that f

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22

Lin, Mei-Shu, and 林美淑. "In vitro Study on The Efficacies of Antacids and Their Effect on The Disintegration of Enteric Coated Tablets." Thesis, 1996. http://ndltd.ncl.edu.tw/handle/72499464818534038893.

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碩士<br>國立臺灣大學<br>藥學研究所<br>84<br>The purpose of this study is to investigate the influence of antacids on the disintegration of enteric coated drugs. The antacids and enteric coated tablets are collected from National Taiwan University Hospital. The quality of the antacids, in terms of preliminary antacid test (PAT) and neutralizing capacity (ANC) , as well as the quality of the enteric coated tablets, in terms of disintegration time were tested according to USP XXIII. In addition, the buffer

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23

Ley, Ludwin. "Vergleich der Pharmakokinetik der intakten und der zerkleinerten 40 mg enteric coated Pantoprazoltablette bei gleichzeitiger Verabreichung von säureneutralisierenden Substanzen bei gesunden Probanden." 2004. http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&doc_number=014188941&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA.

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24

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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25

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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26

Liu, Jiping 1971. "Applications of cellulose acetate phthalate aqueous dispersion (Aquacoat CPD) for enteric coatin." 2001. http://hdl.handle.net/2152/10724.

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