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https://doi.org/10.2478/v10007-007-0048-y

Solid dispersion of meloxicam: Factorially designed dosage form for geriatric population

DEEPA PATHAK
SUNITA DAHIYA
KAMLA PATHAK

Puni tekst: engleski, pdf (261 KB) str. 99-110 preuzimanja: 1.856* citiraj
APA 6th Edition
PATHAK, D., DAHIYA, S. i PATHAK, K. (2008). Solid dispersion of meloxicam: Factorially designed dosage form for geriatric population. Acta Pharmaceutica, 58 (1), 99-110. https://doi.org/10.2478/v10007-007-0048-y
MLA 8th Edition
PATHAK, DEEPA, et al. "Solid dispersion of meloxicam: Factorially designed dosage form for geriatric population." Acta Pharmaceutica, vol. 58, br. 1, 2008, str. 99-110. https://doi.org/10.2478/v10007-007-0048-y. Citirano 23.10.2019.
Chicago 17th Edition
PATHAK, DEEPA, SUNITA DAHIYA i KAMLA PATHAK. "Solid dispersion of meloxicam: Factorially designed dosage form for geriatric population." Acta Pharmaceutica 58, br. 1 (2008): 99-110. https://doi.org/10.2478/v10007-007-0048-y
Harvard
PATHAK, D., DAHIYA, S., i PATHAK, K. (2008). 'Solid dispersion of meloxicam: Factorially designed dosage form for geriatric population', Acta Pharmaceutica, 58(1), str. 99-110. https://doi.org/10.2478/v10007-007-0048-y
Vancouver
PATHAK D, DAHIYA S, PATHAK K. Solid dispersion of meloxicam: Factorially designed dosage form for geriatric population. Acta Pharm. [Internet]. 2008 [pristupljeno 23.10.2019.];58(1):99-110. https://doi.org/10.2478/v10007-007-0048-y
IEEE
D. PATHAK, S. DAHIYA i K. PATHAK, "Solid dispersion of meloxicam: Factorially designed dosage form for geriatric population", Acta Pharmaceutica, vol.58, br. 1, str. 99-110, 2008. [Online]. https://doi.org/10.2478/v10007-007-0048-y

Sažetak
The objective of the present work was to improve the dissolution properties of the poorly water-soluble drug meloxicam by preparing solid dispersions with hydroxyethylcellulose (HEC), mannitol and polyethylene glycol (PEG) 4000 and to develop a dosage form for geriatric population. Differential scanning calorimetry, X–ray diffractometry, Fourier transform infrared spectroscopy and scanning electron microscopy were used to investigate the solid-state physical structure of the prepared solid dispersions. Higher in vitro dissolution of solid dispersions was recorded compared to their corresponding physical mixtures and the pure drug. PEG 4000 in 1:9 drug to carrier ratio exhibited the highest drug release (100.2%), followed by mannitol (98.2%) and HEC (89.5%) in the same ratio. Meloxicam-PEG 4000 solid dispersion was formulated into suspension and optimization was carried out by 23 factorial design. Formulations containing higher levels of methyl cellulose and higher levels of either sodium citrate or Tween 80 exhibited the highest drug release.

Ključne riječi
meloxicam; solid dispersion; hydroxyethylcellulose; mannitol; polyethylene glycol 4000; 23 factorial design; geriatric formulation

Hrčak ID: 17849

URI
https://hrcak.srce.hr/17849

[hrvatski]

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