Synthesis, characterization and comparison of novel poly (sebacic anhydride) biopolymeric implants and microspheres for the controlled release of an anticancer drug (Record no. 17360)

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control field 20220829161728.0
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040 ## - CATALOGING SOURCE
Original cataloging agency AIKTC-KRRC
Transcribing agency AIKTC-KRRC
100 ## - MAIN ENTRY--PERSONAL NAME
9 (RLIN) 17657
Author Kala, Shabari Girinath
245 ## - TITLE STATEMENT
Title Synthesis, characterization and comparison of novel poly (sebacic anhydride) biopolymeric implants and microspheres for the controlled release of an anticancer drug
250 ## - EDITION STATEMENT
Volume, Issue number Vol.56(2), Apr-June
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Place of publication, distribution, etc. Karnataka
Name of publisher, distributor, etc. Association of Pharmaceutical Teachers of India (APTI)
Year 2022
300 ## - PHYSICAL DESCRIPTION
Pagination 429-437p.
520 ## - SUMMARY, ETC.
Summary, etc. Aim: The purpose of this study was to investigate the comparative drug release kinetics
of implants and microspheres of an anticancer drug loaded onto a bio-degradable polymer.
Methods: Poly (sebacic anhydride) was synthesized using a melt-polycondensation
reaction, and its physicochemical properties were determined using gel permeation
chromatography, nuclear magnetic resonance, differential scanning calorimetry, and
Fourier transform infrared techniques. The polymer was used to encapsulate drugs via
the melt moulding technique for implants and the solvent evaporation technique for
microspheres. Results:
In-vitro degradation of implants showed a 95% degradation rate
in 6 days with the disappearance of the anhydride peak due to polymer hydrolysis.
The microspheres of size 63 ± 3 μm were found to be spherical and porous in optical
microscopy images
. In-vitro drug release from implants (85 ± 3.5%) and microspheres
(88 ± 4.5%) in pH 7.4 revealed similar sustained drug release following Higuchi kinetics.
Conclusion: There was no significant difference observed in drug release patterns from
implants and microspheres with the same quantity of polymer. Therefore, poly (sebacic
anhydride) could become a successful candidate for controlling the release of a drug over
a long period of time.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
9 (RLIN) 4639
Topical term or geographic name entry element PHARMACEUTICS
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9 (RLIN) 17658
Co-Author Chinni, Santhivardhan
773 0# - HOST ITEM ENTRY
Title Indian journal of pharmaceutical education and research
International Standard Serial Number 0019-5464
Place, publisher, and date of publication Bengluru Association of Pharmaceutical Teachers of India (APTI)
856 ## - ELECTRONIC LOCATION AND ACCESS
URL https://www.ijper.org/sites/default/files/IndJPhaEdRes-56-2-429.pdf
Link text Click here
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Source of classification or shelving scheme
Koha item type Articles Abstract Database
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Withdrawn status Lost status Source of classification or shelving scheme Damaged status Not for loan Permanent Location Current Location Shelving location Date acquired Barcode Date last seen Price effective from Koha item type
          School of Pharmacy School of Pharmacy Archieval Section 2022-08-29 2022-1427 2022-08-29 2022-08-29 Articles Abstract Database
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