| 000 -LEADER |
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| fixed length control field |
a |
| 003 - CONTROL NUMBER IDENTIFIER |
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| control field |
OSt |
| 005 - DATE AND TIME OF LATEST TRANSACTION |
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| control field |
20211221110711.0 |
| 008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION |
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| fixed length control field |
211221b xxu||||| |||| 00| 0 eng d |
| 040 ## - CATALOGING SOURCE |
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| Original cataloging agency |
AIKTC-KRRC |
| Transcribing agency |
AIKTC-KRRC |
| 100 ## - MAIN ENTRY--PERSONAL NAME |
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| 9 (RLIN) |
14909 |
| Author |
Kathpalia, Harsha |
| 245 ## - TITLE STATEMENT |
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| Title |
Formulation and Optimization of Atovaquone Micronized Suspension by Top-down Method |
| 250 ## - EDITION STATEMENT |
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| Volume, Issue number |
Vol.55(1), Jan-Man |
| 260 ## - PUBLICATION, DISTRIBUTION, ETC. |
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| Place of publication, distribution, etc. |
Karnataka |
| Name of publisher, distributor, etc. |
Association of Pharmaceutical Teachers of India (APTI) |
| Year |
2021 |
| 300 ## - PHYSICAL DESCRIPTION |
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| Pagination |
77-85p. |
| 520 ## - SUMMARY, ETC. |
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| Summary, etc. |
Aim: The present work aimed to tackle the solubility issue of a Biopharmaceutics Classification System (BCS) II drug, Atovaquone. Methods: Formulation of micronized suspension of atovaquone was optimized by employing a 32 full factorial design keeping poloxamer 188 (wetting agent) and phospholipon 90H (stabilizer) as the influential variables affecting the dependent variables viz. particle size and polydispersity index (PdI). Selected formulations from the optimized design space were further evaluated for dissolution and the formulation exhibiting maximum dissolution within 120 min was selected. The optimized batch consisting of atovaquone (15%), poloxamer 188 (2%), phospholipon 90H (1%), glycerin (10%) in the aqueous vehicle was microfluidized. Results: The particle size of resultant suspension was Zavg = 1313 ± 40 nm and PdI =0.1± 0.05. The zeta potential of the final micronized suspension was 0.0555 mV which indicated steric stabilization of the particles. The micronized suspension was adsorbed on a mixture of Kollidon CL SF and Aerosil 200 (2:1) and then dried and passed through 40# sieve. Conclusion: The solid-state characterization of the formulation revealed that the crystalline nature of the drug was retained after the milling process. The saturation solubility and in-vitro dissolution of adsorbed micronized suspension were 2.3-fold times enhanced as compared to the pure drug suspension due to a reduction in particle size. The top-down approach can be employed to improve the poor aqueous solubility of atovaquone. |
| 650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM |
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| 9 (RLIN) |
4639 |
| Topical term or geographic name entry element |
PHARMACEUTICS |
| 700 ## - ADDED ENTRY--PERSONAL NAME |
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| 9 (RLIN) |
14910 |
| Co-Author |
Das, Sukanya |
| 773 0# - HOST ITEM ENTRY |
|---|
| International Standard Serial Number |
0019-5464 |
| Title |
Indian journal of pharmaceutical education and research |
| 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_55_1_77.pdf |
| Link text |
Click here |
| 942 ## - ADDED ENTRY ELEMENTS (KOHA) |
|---|
| Source of classification or shelving scheme |
|
| Koha item type |
Articles Abstract Database |
