Synthesis and in vitro drug release studies on substituted polyphosphazene conjugates of lumefantrine

Authors

  • Sahil Kumar School of Pharmacy & Emerging Sciences, Baddi University of Emerging Sciences & Technology, Baddi-173205, India
  • AlkaSharma School of Pharmacy & Emerging Sciences, Baddi University of Emerging Sciences & Technology, Baddi-173205, India
  • Rajesh K Singh Department of Pharmaceutical Chemistry, Shivalik College of Pharmacy, Nangal, Distt. Roopnagar, Punjab, 140126, India
  • DN Prasad Department of Pharmaceutical Chemistry, Shivalik College of Pharmacy, Nangal, Distt. Roopnagar, Punjab, 140126, India
  • TR Bhardwaj School of Pharmacy & Emerging Sciences, Baddi University of Emerging Sciences & Technology, Baddi-173205, India

Keywords:

polyphosphazene, lumefantrine, conjugate, malaria, p-amino benzoic acid ester

Abstract

The present study pertains to the delivery of antimalarial drug (Lumifantrine). In this, polyphosphazene has been used in the synthesis of polyphosphazene-linked conjugates of Lumifantrine. These polymer-linked Conjugates have been synthesized and characterized by modern analytical techniques. The in-vitro drug release of Lumifantrine drug conjugates: p-Amino benzoic acid ester substituted polyphosphazene drug conjugate (15) and Glycine methyl ester substituted polyphosphazene drug conjugate (21) have been found to be 6.00 % and 5.96% (pH 1.2), 88.52% and 79.86% (pH7.4), respectively. These drugs conjugate may prove an effective delivery system for the treatment of malaria.

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Published

2017-06-30

How to Cite

Sahil Kumar, AlkaSharma, Rajesh K Singh, DN Prasad, & TR Bhardwaj. (2017). Synthesis and in vitro drug release studies on substituted polyphosphazene conjugates of lumefantrine. International Journal of Drug Delivery, 9(2), 36–46. Retrieved from https://ijdd.arjournals.org/index.php/ijdd/article/view/308

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Section

Original Research Articles