CODESTM drug delivery: design and evaluation of metronidazole tablets (Record no. 16971)

000 -LEADER
fixed length control field a
003 - CONTROL NUMBER IDENTIFIER
control field OSt
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20220629155136.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 220629b xxu||||| |||| 00| 0 eng d
040 ## - CATALOGING SOURCE
Original cataloging agency AIKTC-KRRC
Transcribing agency AIKTC-KRRC
100 ## - MAIN ENTRY--PERSONAL NAME
9 (RLIN) 16911
Author Derfla, A. P.
245 ## - TITLE STATEMENT
Title CODESTM drug delivery: design and evaluation of metronidazole tablets
250 ## - EDITION STATEMENT
Volume, Issue number Vol.15(4), Oct-Dec
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Place of publication, distribution, etc. M P
Name of publisher, distributor, etc. BRNSS Publication Hub.
Year 2021
300 ## - PHYSICAL DESCRIPTION
Pagination 400-405p.
520 ## - SUMMARY, ETC.
Summary, etc. Aim: The present study aimed to develop and demonstrate the study of combined effects of biodegradable polymer
coated with different pH-sensitive polymers in the formulation of Metronidazole tablets for colon targeted drug
delivery. Materials and Methods: Metronidazole Hydrochloride is cored with various proportions of biodegradable
polymers such as xanthan gum and chitosan. Then, the double-layered system was designed based on pH-sensitive
eudragit S100 and eudragit L100 as an inner layer and outer layer, respectively. To evaluate the in-vitro dissolution
profile of CODESTM tablets in gastrointestinal fluids, the test was performed using three consecutive media and
drug release kinetics are performed. The drug excipient interaction of CODESTM formulation was characterized
by Fourier transform infrared (FT-IR). Results and Discussion: From the in-vitro drug release studies, F6 tablets
were considered as the optimized formulation, which retard the drug release in the stomach (pH 1.2) and small
intestine (pH 7.4) and progressively increase the release of 75.75% in the colon (pH 6.8) due to mucoadhesive
properties of chitosan. The FT-IR analysis shows that there is no interaction between drug and excipient. The drug
release kinetics followed supercase – II transport with erosion mechanism. Conclusion: Briefly to conclude that
CODESTM technology is a promising method for approach to deliver drug to colon due to the controlled release of
biodegradable polysaccharides and gastric resistance polymer.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
9 (RLIN) 4755
Topical term or geographic name entry element PHARMACOGNOSY
700 ## - ADDED ENTRY--PERSONAL NAME
9 (RLIN) 16904
Co-Author Subramanian, S.
773 0# - HOST ITEM ENTRY
Title International journal of green pharmacy
Place, publisher, and date of publication Mandsaur B.R. Nahata Smriti Sansthan
856 ## - ELECTRONIC LOCATION AND ACCESS
URL https://www.greenpharmacy.info/index.php/ijgp/article/view/3187
Link text Click here
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Source of classification or shelving scheme
Koha item type Articles Abstract Database
Holdings
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 2022-06-29 2022-0968 2022-06-29 2022-06-29 Articles Abstract Database
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