Intradermal vaccination with hollow microneedles: A comparative study of various protein antigen and adjuvant encapsulated nanoparticles

J Control Release. 2017 Nov 28;266:109-118. doi: 10.1016/j.jconrel.2017.09.021. Epub 2017 Sep 21.

Abstract

In this study, we investigated the potential of intradermal delivery of nanoparticulate vaccines to modulate the immune response of protein antigen using hollow microneedles. Four types of nanoparticles covering a broad range of physiochemical parameters, namely poly (lactic-co-glycolic) (PLGA) nanoparticles, liposomes, mesoporous silica nanoparticles (MSNs) and gelatin nanoparticles (GNPs) were compared. The developed nanoparticles were loaded with a model antigen (ovalbumin (OVA)) with and without an adjuvant (poly(I:C)), followed by the characterization of size, zeta potential, morphology, and loading and release of antigen and adjuvant. An in-house developed hollow-microneedle applicator was used to inject nanoparticle suspensions precisely into murine skin at a depth of about 120μm. OVA/poly(I:C)-loaded nanoparticles and OVA/poly(I:C) solution elicited similarly strong total IgG and IgG1 responses. However, the co-encapsulation of OVA and poly(I:C) in nanoparticles significantly increased the IgG2a response compared to OVA/poly(I:C) solution. PLGA nanoparticles and liposomes induced stronger IgG2a responses than MSNs and GNPs, correlating with sustained release of the antigen and adjuvant and a smaller nanoparticle size. When examining cellular responses, the highest CD8+ and CD4+ T cell responses were induced by OVA/poly(I:C)-loaded liposomes. In conclusion, the applicator controlled hollow microneedle delivery is an excellent method for intradermal injection of nanoparticle vaccines, allowing selection of optimal nanoparticle formulations for humoral and cellular immune responses.

Keywords: Adjuvant; Antigen; Hollow microneedles; Intradermal vaccination; Nanoparticles.

Publication types

  • Comparative Study

MeSH terms

  • Adjuvants, Immunologic / administration & dosage*
  • Animals
  • Antigens / administration & dosage*
  • Antigens / chemistry
  • Drug Liberation
  • Female
  • Injections, Intradermal
  • Lactic Acid / administration & dosage
  • Lactic Acid / chemistry
  • Liposomes
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Microinjections
  • Nanoparticles / administration & dosage*
  • Nanoparticles / chemistry
  • Needles*
  • Ovalbumin / administration & dosage*
  • Ovalbumin / chemistry
  • Poly I-C / administration & dosage*
  • Poly I-C / chemistry
  • Polyglycolic Acid / administration & dosage
  • Polyglycolic Acid / chemistry
  • Polylactic Acid-Polyglycolic Acid Copolymer
  • Vaccination / instrumentation*
  • Vaccination / methods

Substances

  • Adjuvants, Immunologic
  • Antigens
  • Liposomes
  • Polylactic Acid-Polyglycolic Acid Copolymer
  • Polyglycolic Acid
  • Lactic Acid
  • Ovalbumin
  • Poly I-C