Development and characterization of anti-diabetic liposomal formulation (Record no. 17583)

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fixed length control field a
003 - CONTROL NUMBER IDENTIFIER
control field OSt
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20220921144305.0
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fixed length control field 220921b xxu||||| |||| 00| 0 eng d
040 ## - CATALOGING SOURCE
Original cataloging agency AIKTC-KRRC
Transcribing agency AIKTC-KRRC
100 ## - MAIN ENTRY--PERSONAL NAME
9 (RLIN) 18003
Author Patil, Anasuya
245 ## - TITLE STATEMENT
Title Development and characterization of anti-diabetic liposomal formulation
250 ## - EDITION STATEMENT
Volume, Issue number Vol.16(1), Jan-Mar
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Place of publication, distribution, etc. M P
Name of publisher, distributor, etc. BRNSS Publication Hub.
Year 2022
300 ## - PHYSICAL DESCRIPTION
Pagination 94-105p.
520 ## - SUMMARY, ETC.
Summary, etc. Introduction: Diabetes is a chronic health condition that affects how human body turns food into energy. It is most commonly occurring disease. Liposomal technology has been employed for the flourishing encapsulation of various drug molecules and oral route of administration is much more convenient. The main aim was to develop and characterize oral antidiabetic liposomal formulation. Further, prepared liposomal formulations evaluated for particle size, % drug release, differential scanning calorimetry (DSC), Fourier transform infrared, in vitro release, release kinetics model, animal studies, and experimental data subjected to statistical testing using one-way analysis of variance followed by Dunnett test were carried out. Materials and Methods: The liposomal formulations were formulated using thin-film hydration technique. Sitagliptin liposomal formulations (F1-F6) were prepared by employing soy lecithin and cholesterol in varying concentration. Results: In vitro release of different antidiabetic liposomal formulations was performed and observed through cellophane membrane using Franz Diffusion cell. The finalized liposomal formulation (F6) showed better release. To check the antihyperglycemic activity was performed using oral glucose tolerance test using Sprague Dawley (SD) rats for the optimized formulation. Finalized formulation (F6) elicited the better in-vitro release 87.85% at 8 h in comparison with the pure drug release was initiate to be 59.57%. Particle size distribution and zeta potential were found to be 40 nm as well as 40 mV, respectively. In vitro release kinetic models were shown that it follows first-order kinetics and high regression coefficient r2 value was 0.975. The DSC thermogram of sitagliptin was found 221.7°C. The DSC thermogram of physical mixture of cholesterol along with soy lecithin was found to be 42.1°C and 220.3°C. DSC analysis confirmed that there was negative interaction between the drug and excipients. Discussion and Conclusion: It would be concluded that antidiabetic liposomal formulation using sitagliptin as drug, soy lecithin and cholesterol as polymer can be formulated thereby can enhance oral bio-availability. The optimized formulation (F6) has shown best formulation based on the in vitro drug release. In vivo studies for the optimized formulation (F6) observed that sitagliptin was found to be more potent than sitagliptin marketed formulation and activity was persisted till 4 h.
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) 18004
Co-Author Rachel, K. Florence
773 0# - HOST ITEM ENTRY
Title International journal of green pharmacy
Place, publisher, and date of publication Mandsaur B.R. Nahata Smriti Sansthan
International Standard Serial Number 0973-8258
856 ## - ELECTRONIC LOCATION AND ACCESS
URL https://www.greenpharmacy.info/index.php/ijgp/article/view/3221
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 2022-09-21 2022-1685 2022-09-21 2022-09-21 Articles Abstract Database
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