Abstract
Single-administration vaccine delivery systems are intended to improve the efficiency and efficacy of immunisation programs in both human and veterinary medicine. In this work, an osmotically triggered delayed delivery device was developed that was able to release a payload after a delay of approximately 21 days, in a consistent and reproducible manner. The device was constructed out of a flexible poly(ε-caprolactone) photo-cured network fabricated into a hollow tubular shape, which expelled approximately 10% of its total payload within 2 days after bursting. Characterisation of the factors that control the delay of release demonstrated that it was advantageous to adjust material permeability and device wall thickness over manipulation of the osmogent concentration in order to maintain reproducibility in burst delay times. The photo-cured poly(ε-caprolactone) network was shown to be fully degradable in vitro, and there was no evidence of cytotoxicity after 11 days of direct contact with primary dermal fibroblasts. This study provides strong evidence to support further development of flexible biomaterials with the aim of continuing improvement of the device burst characteristics in order to provide the greatest chance of the devices succeeding with in vivo vaccine booster delivery.
Highlights
Immunisation is regarded as one of the most successful and cost-effective forms of medical intervention, with vaccinations preventing an estimated 2.5 million deaths worldwide and saving millions of dollars in health care costs per year [1,2,3,4]
Access to common vaccines is regarded by the World Health Organisation (WHO) as a critical component of a well-functioning health care system, and the availability of immunisation is classed as a core component of the human right to health [1,5]
(Mn = 45,000 g/mol), methacrylic anhydride (MAAh), sodium hydroxide pellets (NaOH), and magnesium sulphate (MgSO4 ) were acquired from Sigma Aldrich (Gillingham, UK); potassium carbonate (K2 CO3 ), toluene, dichloromethane (DCM), and hexane were obtained from Fisher Scientific (Loughborough, UK)
Summary
Immunisation is regarded as one of the most successful and cost-effective forms of medical intervention, with vaccinations preventing an estimated 2.5 million deaths worldwide and saving millions of dollars in health care costs per year [1,2,3,4]. Access to common vaccines is regarded by the World Health Organisation (WHO) as a critical component of a well-functioning health care system, and the availability of immunisation is classed as a core component of the human right to health [1,5]. Vaccines produce their prophylactic effect by inducing a pathogen-specific immune response to an antigen that primes the body’s immune system and generates lasting immunological memory, enabling an efficient secondary immune response when the stimulus is encountered again in the future [6]. In the case of wildlife [9], the animal may need to be kept in captivity or recaptured to administer future doses, introducing further expense and complications
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