Encapsulation-free controlled release: Electrostatic adsorption eliminates the need for protein encapsulation in PLGA nanoparticles

Malgosia M Pakulska, Irja Elliott Donaghue, Jaclyn Obermeyer, Anup Tuladhar, Christopher K McLaughlin, Tyler Shendruk, Molly S Shoichet

Research output: Contribution to journalArticlepeer-review

Abstract

Encapsulation of therapeutic molecules within polymer particles is a well-established method for achieving controlled release, yet challenges such as low loading, poor encapsulation efficiency, and loss of protein activity limit clinical translation. Despite this, the paradigm for the use of polymer particles in drug delivery has remained essentially unchanged for several decades. By taking advantage of the adsorption of protein therapeutics to poly(lactic-co-glycolic acid) (PLGA) nanoparticles, we demonstrate controlled release without encapsulation. In fact, we obtain identical, burst-free, extended-release profiles for three different protein therapeutics with and without encapsulation in PLGA nanoparticles embedded within a hydrogel. Using both positively and negatively charged proteins, we show that short-range electrostatic interactions between the proteins and the PLGA nanoparticles are the underlying mechanism for controlled release. Moreover, we demonstrate tunable release by modifying nanoparticle concentration, nanoparticle size, or environmental pH. These new insights obviate the need for encapsulation and offer promising, translatable strategies for a more effective delivery of therapeutic biomolecules.
Original languageEnglish
Article numbere1600519
JournalScience Advances
Volume2
Issue number5
DOIs
Publication statusPublished - 27 May 2016

Keywords

  • controlled release
  • affinity release
  • drug delivery
  • PLGA
  • protein
  • central nervous system
  • hydrogel

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