WJPR Citation New

  All Since 2020
 Citation  8502  4519
 h-index  30  23
 i10-index  227  96

Login

Best Article Awards

World Journal of Pharmaceutical Research (WJPR) is giving Best Article Award in every Issue for Best Article and Issue Certificate of Appreciation to the Authors to promote research activity of scholar.
Best Paper Award :
Dr. Dhrubo Jyoti Sen
Download Article: Click Here

Search

Track Your Article

Abstract

DESIGN AND DEVELOPMENT OF ROXITHROMYCIN FAST DISSOLVING TABLETS

Malkhan Singh*, Dr. Arun Patel, Mr. Shailendra Patel

Abstract

Background: Roxithromycin is a semi-synthetic macrolide antibiotic with very low aqueous solubility, making dissolution an important formulation challenge. Fast dissolving tablets (FDTs) can provide rapid disintegration in the oral cavity without water and may improve convenience for patients who have difficulty swallowing conventional tablets. Objective: The study aimed to develop and evaluate Roxithromycin fast dissolving tablets using a solid-dispersion approach with PEG 4000 and different superdisintegrants, including sodium starch glycolate, croscarmellose sodium and Gum Karaya. Methods: Preformulation studies included organoleptic examination, solubility testing, loss on drying, melting-point determination, UV spectrophotometry and FTIR analysis. Roxithromycin– PEG 4000 physical mixtures and solid dispersions were prepared at drug: polymer ratios of 1: 1, 1: 2 and 1: 3. Tablets equivalent to 150 mg Roxithromycin were prepared by direct compression and evaluated for powder-flow properties, thickness, hardness, friability, weight variation, drug content, disintegration and in-vitro dissolution. Results: Roxithromycin was soluble in methanol and ethanol and sparingly soluble in water, phosphate buffer pH 6.8, 0.1 N HCl, 0.1 N NaOH and chloroform. Loss on drying was 0.175 ± 0.005% and melting point was 118–120°C. The reported 1: 1 drug: PEG 4000 solid dispersion was selected for subsequent tablet development. Powder blends showed bulk density of 0.354–0.368 g/mL, tapped density of 0.458–0.472 g/mL, Carr‟s index of 20.306–23.377% and Hausner‟s ratio of 1.255–1.305. Tablet hardness was 3.2–3.4 kg/cm², friability 0.685–0.821%, thickness 2.8–2.9 mm and drug content 98.45– 99.74%. Formulation F5 showed the shortest reported disintegration time (62 ± 4 s).

Keywords: Roxithromycin; fast dissolving tablet; orally disintegrating tablet; solid dispersion; PEG 4000; superdisintegrant; Gum Karaya; dissolution.


[Full Text Article]  [Download Certificate]

Call for Paper

World Journal of Pharmaceutical Research (WJPR)
Read More

Email & SMS Alert

World Journal of Pharmaceutical Research (WJPR)
Read More

Article Statistics

World Journal of Pharmaceutical Research (WJPR)
Read More

Online Submission

World Journal of Pharmaceutical Research (WJPR)
Read More