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Evaluation of silicone elastomers for tablet coating / (Record no. 12933)

MARC details
000 -LEADER
fixed length control field 03949nam a22003257i 4500
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20210310134032.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 210310s2003 a|||| mb|| 00| 0 eng d
040 ## - CATALOGING SOURCE
Original cataloging agency EG-NcFUE
Language of cataloging eng
Modifying agency EG-NcFUE
Description conventions rda
082 04 - DEWEY DECIMAL CLASSIFICATION NUMBER
Edition number 23
Classification number 615.19005
Item number S.N.E
100 1# - MAIN ENTRY--PERSONAL NAME
Personal name Schulze Nahrup, Julia
Relator term author.
245 10 - TITLE STATEMENT
Title Evaluation of silicone elastomers for tablet coating /
Statement of responsibility, etc by Julia Schulze Nahrup ; Supervisor : ph.D. Adel sakr, ph.D. Hussein Al Khalidi, ph.D. James E. Mark, ph.d. Gerald B. Kasting, ph.D. Randall R. Wickett.
264 #0 - PUBLICATION, DISTRIBUTION, ETC. (IMPRINT)
Date of publication, distribution, etc 2003
300 ## - PHYSICAL DESCRIPTION
Extent viii, 157 leaves :
Other physical details illustrations ;
Dimensions 29 cm
336 ## - CONTENT TYPE
Source rdacontent
Content type term text
Content type code txt
337 ## - MEDIA TYPE
Source rdamedia
Media type term unmediated
Media type code n
338 ## - CARRIER TYPE
Source rdacarrier
Carrier type term volume
Carrier type code nc
502 ## - DISSERTATION NOTE
Dissertation note Thesis (Ph.D.)--University of Cincinnati, 2003
504 ## - BIBLIOGRAPHY, ETC. NOTE
Bibliography, etc Includes bibliographical references
520 ## - SUMMARY, ETC.
Summary, etc The objective of this project was to study the effect of modifications of endhydroxylated poly(dimethylsiloxane) (PDMS) formulations on tablet drug release. Emulsions of crosslinked endhydroxylated PDMS, a novel film-forming polymer, were characterized and investigated for their ability to be applied onto tablet cores in a spray-coating process for controlled drug release. Modifications of the crosslinking agent from the most commonly used tetraethylorthosilicate (TEOS) to the trifunctional 3-(2,3-epoxypropoxy)propyltrimethoxysilane (SIG) and a 1:1-mixture of the two crosslinker were undertaken. Addition of vermiculate clay, copolymeric substances and different channeling-agents were studied. Copolymers of methylpolysiloxane with polyoxyethylene (DC193 and DC5324) or dimethyl, methyl (polyoxyethylene) (DCQ2-5220) as well as poly (acrylamide-co-acrylic acid) were used. Lactose, microcrystalline cellulose (MCC) and polyethyleneglycol 8000 (PEG) were the channeling-agents applied. A change in molecular weight of the PDMS was analyzed. Effects on dispersion properties were characterized by particle size distribution, viscosity and visual observation of phase-separation. Mechanical properties of resulting cast and sprayed films were studied to determine applicability in a pan-coating process. Release of Hydrochlorothiazide (marker-drug) was studied from tablets coated in a lab-size conventional coating pan. Dispersions were found suitable for a spray-coating process. Only the formulation with acrylic-copolymer addition was unstable as phase separation occurred. Preparation of free films showed that methylpolysiloxane-copolymers negatively affected the mechanical properties so that coating onto tablet cores was not possible. Tablets coated with formulations crosslinked using the 1:1-mixture of SIG/TEOS and containing polyethyleneglycol were most suitable to control drug release, at 5% coating weight. Constant release rates were achieved for formulations with up to 25% (w/w of PDMS) PEG; higher amounts resulted in a non-linear release pattern. Upon adding 50% PEG, a drug release of 62% over 24 hours could be achieved. Formulations containing 25 and 50% (w/w of PDMS) PEG were stable for at least 3 months when tested according to ICH-guidelines. In comparison with Eudragit NE (copolymeric product of 2:1 ethylacrylate / methylmethacrylate) PDMS-formulations showed similar mechanical and improved spray-application properties. Addition of channeling agents was necessary for both products to achieve drug release. The effect of polyethyleneglycol was greater on formulations based on PDMS than for Eudragit NE.
610 20 - SUBJECT ADDED ENTRY--CORPORATE NAME
Corporate name or jurisdiction name as entry element University of Cincinnati
General subdivision Theses. Ph.D. (Pharmaceutical Sciences) 2003.
9 (RLIN) 33866
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element Pharmaceutical technology
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element Pharmaceutical industry
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Al Khalidi, Hussein,
Relator term supervisor.
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Sakr, Adel Mohamed,
Relator term supervisor.
9 (RLIN) 33831
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Mark, James E.,
Relator term supervisor.
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Kasting, Gerald B.,
Relator term supervisor.
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Wickett, Randall R.,
Relator term supervisor.
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Source of classification or shelving scheme Dewey Decimal Classification
Koha item type Thesis
Holdings
Lost status Source of classification or shelving scheme Damaged status Not for loan Collection code Home library Current library Shelving location Date acquired Source of acquisition Acquisition method Total Checkouts Full call number Barcode Date last seen Copy number Price effective from Koha item type
  Dewey Decimal Classification     Pharmacy ( Pharmaceutical Technology ) Main library Main library C5 PHD 10/03/2021 Prof. Dr. Adel Sakr Lib Donation 2021   615.19005 S.N.E 00016474 20/02/2025 c.1 10/03/2021 Thesis