2014
DOI: 10.1007/978-1-4939-1417-3_12
|View full text |Cite
|
Sign up to set email alerts
|

Implants as Sustained Release Delivery Devices for Vaccine Antigens

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

0
6
0

Year Published

2015
2015
2022
2022

Publication Types

Select...
4

Relationship

0
4

Authors

Journals

citations
Cited by 4 publications
(6 citation statements)
references
References 52 publications
(83 reference statements)
0
6
0
Order By: Relevance
“…Experiments with the Georgia Institute of Technology patch and other dermal patches under development demonstrate immune responses comparable with the standard modes of injectable delivery [64,90,91]. There has also been considerable interest in exploring additional vaccine-delivery innovations such as sustainedrelease formulations and skin permeabilization techniques which could potentially be applicable for IPV and substantially reduce logistical challenges of IPV administration [65,66,92]. Proof-ofconcept information in humans with such devices and methods should be the next logical step, and …”
Section: Colombia-dominican Republicguatemala-panama India Bangladeshmentioning
confidence: 95%
“…Experiments with the Georgia Institute of Technology patch and other dermal patches under development demonstrate immune responses comparable with the standard modes of injectable delivery [64,90,91]. There has also been considerable interest in exploring additional vaccine-delivery innovations such as sustainedrelease formulations and skin permeabilization techniques which could potentially be applicable for IPV and substantially reduce logistical challenges of IPV administration [65,66,92]. Proof-ofconcept information in humans with such devices and methods should be the next logical step, and …”
Section: Colombia-dominican Republicguatemala-panama India Bangladeshmentioning
confidence: 95%
“…The degradation or swelling of the polymer results in a slow‐release of the antigen (Engert, 2015). The choice of polymer primarily includes silicone, ethylene‐vinyl acetate co‐polymer, collagen, or PLGA (Engert, 2015). Furthermore, additives or excipients such as PEG are added as a pore‐forming agent (or porogen) to fine‐tune the release profile of the antigen (Herrmann et al, 2007; Schulze & Winter, 2009).…”
Section: Slow‐release Systemsmentioning
confidence: 99%
“…Furthermore, additives or excipients such as PEG are added as a pore‐forming agent (or porogen) to fine‐tune the release profile of the antigen (Herrmann et al, 2007; Schulze & Winter, 2009). Implants are prepared by different techniques like direct compression, melting/molding, extrusion and casting (Engert, 2015). Implantable systems have been extensively used for hormonal treatments, birth control, ocular treatment and controlled drug release (Engert, 2015; Palomba et al, 2012).…”
Section: Slow‐release Systemsmentioning
confidence: 99%
See 1 more Smart Citation
“…Implants generally need to be given by injection, which is not preferred by patients and may be more complex and expensive to manufacture [10]. From a vaccine perspective, implants provide a single-shot approach reducing the need for booster doses, which are commonly required for traditional non-living vaccines in order to stimulate long-lasting immunity [11]. Unlike most drug implants, vaccine implants usually require the relatively short-term release of vaccine components in order to induce potent immune responses while avoiding tolerance (low doses of antigen for an extended period of time) or sequestration and/or deletion (higher amounts of antigen over an extended period of time) of lymphocytes [12].…”
Section: Introductionmentioning
confidence: 99%