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Preparation of sirna-encapsulated plga nanoparticles for sustained release of sirna and evaluation of encapsulation efficiency

  • Panayotis Pantazis
  • , Konstantinos Dimas
  • , James H. Wyche
  • , Shrikant Anant
  • , Courtney W. Houchen
  • , Jayanth Panyam
  • , Rama P. Ramanujam

Research output: Chapter in Book/Report/Conference proceedingChapter

Abstract

Nanoparticles (NPs) formulated using poly (d,l-lactide-co-glycolide) (PLGA), a biodegradable, biocompatible, and clinically approved polymer, have been widely used for targeted drug delivery. Here we provide methods for preparing PLGA NPs that encapsulate small interfering RNA (siRNA). The siRNA NPs are formulated using a double-emulsion solvent evaporation technique with the addition of a small amount of the cationic polymer, polyethyleneimine, which significantly increases siRNA encapsulation.

Original languageEnglish (US)
Title of host publicationNanoparticles in Biology and Medicine
Subtitle of host publicationMethods and Protocols
EditorsMikhail Soloviev
Pages311-319
Number of pages9
DOIs
StatePublished - 2012

Publication series

NameMethods in Molecular Biology
Volume906
ISSN (Print)1064-3745

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Cancer therapy
  • Cancer treatment
  • Drug delivery
  • Nanoparticles
  • Poly(lactic-co-glycolic) acid
  • RNAi
  • siRNA

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