Indexado em
  • Abra o Portão J
  • Genamics JournalSeek
  • Chaves Acadêmicas
  • JournalTOCs
  • Bíblia de pesquisa
  • Infraestrutura Nacional de Conhecimento da China (CNKI)
  • Scimago
  • Diretório de Periódicos de Ulrich
  • Biblioteca de periódicos eletrônicos
  • RefSeek
  • Universidade de Hamdard
  • EBSCO AZ
  • OCLC- WorldCat
  • Catálogo online SWB
  • Biblioteca Virtual de Biologia (vifabio)
  • publons
  • MIAR
  • Serviços de Indexação Científica (SIS)
  • Euro Pub
  • Google Scholar
Compartilhe esta página
Folheto de jornal
Flyer image

Abstrato

Formulation and In-Vitro Evaluation of Piroxicam Loaded BSA Nanospheres by Desolvation

Sravya Neela, Kiran Babu Uppuluri*

Protein nanoparticles offer improved delivery of drugs particularly targeted delivery to specific cells by ligand attachment, sustained and triggered release. Non steroidal anti-inflammatory drug (NSAID), Piroxicam (PRX) is one of the most widely used drug for treating pain and inflammation. But despite its potent analgesic action it has few draw backs like low absorption rate due to poor water solubility and side effects due to non specific inhibition of Cyclooxygenase enzymes. In this context here, we report a new PRX self-assembled nano sphere delivery system developed from bovine serum albumin (BSA) using a very simple, rapid and reliable method, desolvation. Synthesized nanoparticles were characterized by particle size distribution, zeta potential, polydispersity index, FTIR, scanning electron microscopy and in-vitro release studies. The formulated BSA-PRX nano particles exhibited a uniform spherical shape with an average size of 388.7nm. In vitro release behavior of the drug from BSA conjugate suggests that about 50% of the drug was released during first 3h and 85% after 18h.

Isenção de responsabilidade: Este resumo foi traduzido usando ferramentas de inteligência artificial e ainda não foi revisado ou verificado