Publication: Development and characterization of lyophilized diazepam-loaded polymeric micelles
Issued Date
2014-02-01
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15309932
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2-s2.0-84893704496
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Mahidol University
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SCOPUS
Bibliographic Citation
AAPS PharmSciTech. Vol.15, No.1 (2014), 52-64
Suggested Citation
Jiraphong Suksiriworapong, Tanaporn Rungvimolsin, Atitaya A-Gomol, Varaporn Buraphacheep Junyaprasert, Doungdaw Chantasart Development and characterization of lyophilized diazepam-loaded polymeric micelles. AAPS PharmSciTech. Vol.15, No.1 (2014), 52-64. doi:10.1208/s12249-013-0032-4 Retrieved from: https://repository.li.mahidol.ac.th/handle/20.500.14594/34906
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Title
Development and characterization of lyophilized diazepam-loaded polymeric micelles
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Abstract
Polymeric micelles were studied as delivery carriers of diazepam, a practically insoluble drug in water, for rectal administration. The diazepam-loaded polymeric micelles were developed by using poloxamer 407 (P407), poloxamer 188, and d-α-tocopheryl poly(ethylene glycol) 1000 succinate (TPGS). Among the used polymers, TPGS resulted in polymeric micelles with good characteristics for encapsulation of diazepam which had the small particle size of 8-12 nm and narrow size distribution (PI 0.053-0.275). Additionally, 7.5% w/v of TPGS could entirely entrap the desired concentration of diazepam (5 mg/mL). To improve the physical stability upon lyophilization, an addition of P407 of 1% w/v prevented aggregation, increased physical stability, and maintained chemical stability of the lyophilized powders of diazepam-loaded polymeric micelles for 3 months storage at 4 C. The rate and amount of diazepam release from TPGS polymeric micelles mainly depended on the concentration of TPGS. The release data were fitted to Higuchi's model suggesting that the drug release mechanism was controlled by Fickian diffusion. In conclusion, 10% w/v TPGS and 1% w/v P407 were the optimum formulation of lyophilized diazepam-loaded polymeric micelles. © 2013 American Association of Pharmaceutical Scientists.