Novel glibenclamide–phospholipid complex for diabetic treatment: formulation, physicochemical characterization, and in-vivo evaluation (Record no. 17325)

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040 ## - CATALOGING SOURCE
Original cataloging agency AIKTC-KRRC
Transcribing agency AIKTC-KRRC
100 ## - MAIN ENTRY--PERSONAL NAME
9 (RLIN) 17593
Author Rathor, Sandeep
245 ## - TITLE STATEMENT
Title Novel glibenclamide–phospholipid complex for diabetic treatment: formulation, physicochemical characterization, and in-vivo evaluation
250 ## - EDITION STATEMENT
Volume, Issue number Vol.56(3), Jul-Sep
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 697-705p.
520 ## - SUMMARY, ETC.
Summary, etc. Introduction: Formulation of phospholipid complex is an ideal approach to improve the<br/>solubility of poorly soluble drugs. Objectives: This study has been aimed to prepare a novel<br/>glibenclamide-phospholipid complex by using the solvent evaporation technique. Materials<br/>and Methods: Because glibenclamide is a weakly soluble medication, complexing it with<br/>phospholipids is an excellent way to enhance its solubility. The phospholipid complex<br/>of Glibenclamide was produced using the solvent-evaporation technique to enhance its<br/>oral efficacy. The formulation was characterized and evaluated by various parameters<br/>including FTIR, DSC, PXRD, SEM, TEM,<br/>in vitro drug release, and<br/>in vivo pharmacokinetic<br/>studies in Wistar rats plasma. According to studies, the Glibenclamide phosphates<br/>combination is significantly more water-soluble than the physical combination and pure<br/>Glibenclamide. The oral bioavailability of the glibenclamide-phospholipids complex was<br/>measured by using HPLC in Wistar rats’ plasma. Results: There was no substantial<br/>interaction between the medication and the phospholipid in the formulation, according<br/>to the FTIR and PXRD findings. The morphology of the formulation was verified by<br/>SEM and TEM investigations, indicating that the crystalline form had been converted<br/>to an amorphous form. The glibenclamide-phospholipids complex had a greater peak<br/>plasma concentration (5.1 vs. 3.8 g/mL), its AUC was higher (14.65 vs. 11.81 μgh/L),<br/>and its T1/2 was longer (2.4 vs. 3.1 hr), showing that it enhanced drug dissolution<br/>rate. Conclusion: The findings showed that increasing the oral bioavailability of water-<br/>insoluble medicines by phospholipid-complexation is a potential approach. The results<br/>showed that phospholipid-complexation may be used to enhance the oral bioavailability<br/>of water-insoluble drugs.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
9 (RLIN) 4639
Topical term or geographic name entry element PHARMACEUTICS
700 ## - ADDED ENTRY--PERSONAL NAME
9 (RLIN) 17594
Co-Author Bhatt, D.C.
773 0# - HOST ITEM ENTRY
Place, publisher, and date of publication Bengluru Association of Pharmaceutical Teachers of India (APTI)
Title Indian journal of pharmaceutical education and research
International Standard Serial Number 0019-5464
856 ## - ELECTRONIC LOCATION AND ACCESS
URL https://www.ijper.org/sites/default/files/IndJPhaEdRes-56-3-697_0.pdf
Link text Click here
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    Dewey Decimal Classification     School of Pharmacy School of Pharmacy Archieval Section 25/08/2022   2022-1375 25/08/2022 25/08/2022 Articles Abstract Database
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