Stimuli-Responsive Polymeric Systems for Controlled Protein and Peptide Delivery: Future Implications for Ocular Delivery

Molecules. 2016 Jul 30;21(8):1002. doi: 10.3390/molecules21081002.

Abstract

Therapeutic proteins and peptides have become notable in the drug delivery arena for their compatibility with the human body as well as their high potency. However, their biocompatibility and high potency does not negate the existence of challenges resulting from physicochemical properties of proteins and peptides, including large size, short half-life, capability to provoke immune responses and susceptibility to degradation. Various delivery routes and delivery systems have been utilized to improve bioavailability, patient acceptability and reduce biodegradation. The ocular route remains of great interest, particularly for responsive delivery of macromolecules due to the anatomy and physiology of the eye that makes it a sensitive and complex environment. Research in this field is slowly gaining attention as this could be the breakthrough in ocular drug delivery of macromolecules. This work reviews stimuli-responsive polymeric delivery systems, their use in the delivery of therapeutic proteins and peptides as well as examples of proteins and peptides used in the treatment of ocular disorders. Stimuli reviewed include pH, temperature, enzymes, light, ultrasound and magnetic field. In addition, it discusses the current progress in responsive ocular drug delivery. Furthermore, it explores future prospects in the use of stimuli-responsive polymers for ocular delivery of proteins and peptides. Stimuli-responsive polymers offer great potential in improving the delivery of ocular therapeutics, therefore there is a need to consider them in order to guarantee a local, sustained and ideal delivery of ocular proteins and peptides, evading tissue invasion and systemic side-effects.

Keywords: bioavailability; in situ; ocular barriers; ocular delivery; pre-corneal elimination; protein and peptide delivery; stimuli responsive polymer.

Publication types

  • Review

MeSH terms

  • Biological Availability
  • Delayed-Action Preparations
  • Drug Carriers / administration & dosage*
  • Drug Carriers / chemistry
  • Drug Delivery Systems / methods
  • Eye Diseases / drug therapy*
  • Hot Temperature
  • Humans
  • Hydrogen-Ion Concentration
  • Magnetic Fields
  • Peptides / administration & dosage*
  • Peptides / chemistry
  • Peptides / pharmacokinetics
  • Polymers / chemistry*
  • Proteins / administration & dosage*
  • Proteins / chemistry
  • Proteins / pharmacokinetics

Substances

  • Delayed-Action Preparations
  • Drug Carriers
  • Peptides
  • Polymers
  • Proteins