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Pharmacological and toxicological investigations of etodolac loaded gum katira microspheres prepared by W1/O/W2 emulsion solvent evaporation technique in rats
Ruhidas, Biswajit; Ray, Rajat; Naskar, Debjyoti; Chakra, Biplab Kumar; Chatterjee, Tapan Kumar.
Affiliation
  • Ruhidas, Biswajit; Jadavpur University. Department of Pharmaceutical Technology. Kolkata. IN
  • Ray, Rajat; Adamas University. Department of Pharmaceutical Technology. Kolkata. IN
  • Naskar, Debjyoti; Jadavpur University. Department of Pharmaceutical Technology. Kolkata. IN
  • Chakra, Biplab Kumar; Jadavpur University. Department of Pharmaceutical Technology. Kolkata. IN
  • Chatterjee, Tapan Kumar; JIS University. Department of Pharmaceutical Science and Technology. Kolkata. IN
Braz. J. Pharm. Sci. (Online) ; 53(4): e00212, 2017. tab, graf, ilus
Article in English | LILACS | ID: biblio-889429
Responsible library: BR40.1
Localization: BR40.1
ABSTRACT
ABSTRACT Etodolac is a non-steroidal anti-inflammatory drug (NSAID) and approved by USFDA as a COX2 inhibitor. Although etodolac therapy provides clinical benefits, it is associated with upper gastrointestinal (GI) tract complications also. Etodolac loaded gum Katira microsphere (ELGKM) was prepared by W1/O/W2 emulsion solvent evaporation technique. The gastric irritation properties of orally administered pure etodolac, ELGKM and blank microspheres (without etodolac) were evaluated in experimental rats treated for 6 days. The stomach examination and biochemical investigation of stomach tissue of treated rats indicated that ELGKM formulation remarkably reduced ulcerogenecity as compared to pure etodolac. The anti-inflammatory activities of pure etodolac and ELGKMs were ascertained by the implantation of cotton pellets in rats for 6 days. Based on the results, ELGKMs showed significant anti-inflammatory activities (P<0.01) as compared to control group. The cotton pellets test suggested that ELGKM formulation retained more anti-inflammatory properties among the groups. The hematological changes, biochemical analysis and histopathological studies of subacute toxicity in rats revealed that ELGKM were the effective sustained release formulation in the treatment of chronic pain and inflammation. In conclusion, the physicochemical characterization, pharmacological and toxicological studies suggest that ELGKMs may represent as a potential candidate for sustained drug delivery (10-12 hours) in chronic joint pain related diseases with remarkably diminished gastrointestinal side effects.
Subject(s)


Full text: Available Collection: International databases Database: LILACS Main subject: Tragacanth / Evaporation / Etodolac / Microspheres Limits: Animals Language: English Journal: Braz. J. Pharm. Sci. (Online) Journal subject: Farmacologia / Terapˆutica / Toxicologia Year: 2017 Document type: Article / Project document Affiliation country: India Institution/Affiliation country: Adamas University/IN / JIS University/IN / Jadavpur University/IN

Full text: Available Collection: International databases Database: LILACS Main subject: Tragacanth / Evaporation / Etodolac / Microspheres Limits: Animals Language: English Journal: Braz. J. Pharm. Sci. (Online) Journal subject: Farmacologia / Terapˆutica / Toxicologia Year: 2017 Document type: Article / Project document Affiliation country: India Institution/Affiliation country: Adamas University/IN / JIS University/IN / Jadavpur University/IN
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