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Topical dosage form of valdecoxib: Preparation and pharmacological evaluation

K. S. KESAVANARAYANAN
MOHANAVELU NAPPINNAI
RAJU ILAVARASAN

Puni tekst: engleski, pdf (72 KB) str. 199-209 preuzimanja: 1.113* citiraj
APA 6th Edition
KESAVANARAYANAN, K.S., NAPPINNAI, M. i ILAVARASAN, R. (2007). Topical dosage form of valdecoxib: Preparation and pharmacological evaluation. Acta Pharmaceutica, 57 (2), 199-209. Preuzeto s https://hrcak.srce.hr/9852
MLA 8th Edition
KESAVANARAYANAN, K. S., et al. "Topical dosage form of valdecoxib: Preparation and pharmacological evaluation." Acta Pharmaceutica, vol. 57, br. 2, 2007, str. 199-209. https://hrcak.srce.hr/9852. Citirano 27.06.2019.
Chicago 17th Edition
KESAVANARAYANAN, K. S., MOHANAVELU NAPPINNAI i RAJU ILAVARASAN. "Topical dosage form of valdecoxib: Preparation and pharmacological evaluation." Acta Pharmaceutica 57, br. 2 (2007): 199-209. https://hrcak.srce.hr/9852
Harvard
KESAVANARAYANAN, K.S., NAPPINNAI, M., i ILAVARASAN, R. (2007). 'Topical dosage form of valdecoxib: Preparation and pharmacological evaluation', Acta Pharmaceutica, 57(2), str. 199-209. Preuzeto s: https://hrcak.srce.hr/9852 (Datum pristupa: 27.06.2019.)
Vancouver
KESAVANARAYANAN KS, NAPPINNAI M, ILAVARASAN R. Topical dosage form of valdecoxib: Preparation and pharmacological evaluation. Acta Pharm. [Internet]. 2007 [pristupljeno 27.06.2019.];57(2):199-209. Dostupno na: https://hrcak.srce.hr/9852
IEEE
K.S. KESAVANARAYANAN, M. NAPPINNAI i R. ILAVARASAN, "Topical dosage form of valdecoxib: Preparation and pharmacological evaluation", Acta Pharmaceutica, vol.57, br. 2, str. 199-209, 2007. [Online]. Dostupno na: https://hrcak.srce.hr/9852. [Citirano: 27.06.2019.]

Sažetak
Valdecoxib, a selective COX-2 inhibitor, produces serious side effects when given orally. This has led to its withdrawal. Topical application of valdecoxib was formulated and evaluated for its efficacy and safety. Standard procedures were followed and male Wistar albino rats were used to test the anti-inflammatory effect and effect in hyperalgesic conditions. Ointments, creams and gels containing valdecoxib 1 % (m/m) were prepared. These were tested for physical appearance, pH, spreadability, drug content uniformity, in vitro diffusion. Gel prepared using Carbopol 940 (F-X) was selected after the analysis of the results. Formulation F-X was evaluated for acute skin irritancy, anti-inflammatory effect, optimum effective concentration of valdecoxib, effect on hyperalgesia, inhibition of the granulation tissue formation and anti-arthritic effect. Determination of valdecoxib in test animals plasma and determining the blood clotting time and bleeding time were conducted to study the safety of topical valdecoxib.
Valdecoxib gel containing 1 % (m/m) of the drug was significantly (p < 0.05) more effective in inhibiting hyperalgesia associated with inflammation, compared to placebo gel, but exhibited significantly (p < 0.05) lower suppression of inflammation than rofecoxib gel. Concentration of valdecoxib used in the preparation minimizes the risk of systemic effects, as shown by the analysis of rat plasma for the presence of valdecoxib; hence, this may be the alternative to oral preparations. The bleeding and clotting time showed no significant difference before and after application of F-X.

Ključne riječi
valdecoxib; topical gel; in vitro; in vivo evaluation

Hrčak ID: 9852

URI
https://hrcak.srce.hr/9852

[hrvatski]

Posjeta: 1.537 *