TY - JOUR
T1 - Transcutaneously refillable nanofluidic implant achieves sustained level of tenofovir diphosphate for HIV pre-exposure prophylaxis
AU - Chua, Corrine Ying Xuan
AU - Jain, Priya
AU - Ballerini, Andrea
AU - Bruno, Giacomo
AU - Hood, R. Lyle
AU - Gupte, Manas
AU - Gao, Song
AU - Di Trani, Nicola
AU - Susnjar, Antonia
AU - Shelton, Kathryn
AU - Bushman, Lane R.
AU - Folci, Marco
AU - Filgueira, Carly S.
AU - Marzinke, Mark A.
AU - Anderson, Peter L.
AU - Hu, Ming
AU - Nehete, Pramod
AU - Arduino, Roberto C.
AU - Sastry, Jagannadha K.
AU - Grattoni, Alessandro
N1 - Funding Information:
AG discloses a financial interest in NanoMedical Systems, Inc. PLA receives grants and contract work from Gilead Sciences, paid to his institution. All other authors declare no conflict of interest.
Funding Information:
This work was supported by NIH R01 AI120749-01A1 and start-up funds from Houston Methodist Research Institute (AG).
Publisher Copyright:
© 2018 Elsevier B.V.
PY - 2018/9/28
Y1 - 2018/9/28
N2 - Pre-exposure prophylaxis (PrEP) with antiretroviral (ARV) drugs are effective at preventing human immunodeficiency virus (HIV) transmission. However, implementation of PrEP presents significant challenges due to poor user adherence, low accessibility to ARVs and multiple routes of HIV exposure. To address these challenges, we developed the nanochannel delivery implant (NDI), a subcutaneously implantable device for sustained and constant delivery of tenofovir alafenamide (TAF) and emtricitabine (FTC) for HIV PrEP. Unlike existing drug delivery platforms with finite depots, the NDI incorporates ports allowing for transcutaneous refilling upon drug exhaustion. NDI-mediated drug delivery in rhesus macaques resulted in sustained release of both TAF and FTC for 83 days, as indicated by concentrations of TAF, FTC and their respectively metabolites in plasma, PBMCs, rectal mononuclear cells and tissues associated with HIV transmission. Notably, clinically relevant preventative levels of tenofovir diphosphate were achieved as early as 3 days after NDI implantation. We also demonstrated the feasibility of transcutaneous drug refilling to extend the duration of PrEP drug delivery in NHPs. Overall, the NDI represents an innovative strategy for long-term HIV PrEP administration in both developed and developing countries.
AB - Pre-exposure prophylaxis (PrEP) with antiretroviral (ARV) drugs are effective at preventing human immunodeficiency virus (HIV) transmission. However, implementation of PrEP presents significant challenges due to poor user adherence, low accessibility to ARVs and multiple routes of HIV exposure. To address these challenges, we developed the nanochannel delivery implant (NDI), a subcutaneously implantable device for sustained and constant delivery of tenofovir alafenamide (TAF) and emtricitabine (FTC) for HIV PrEP. Unlike existing drug delivery platforms with finite depots, the NDI incorporates ports allowing for transcutaneous refilling upon drug exhaustion. NDI-mediated drug delivery in rhesus macaques resulted in sustained release of both TAF and FTC for 83 days, as indicated by concentrations of TAF, FTC and their respectively metabolites in plasma, PBMCs, rectal mononuclear cells and tissues associated with HIV transmission. Notably, clinically relevant preventative levels of tenofovir diphosphate were achieved as early as 3 days after NDI implantation. We also demonstrated the feasibility of transcutaneous drug refilling to extend the duration of PrEP drug delivery in NHPs. Overall, the NDI represents an innovative strategy for long-term HIV PrEP administration in both developed and developing countries.
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U2 - 10.1016/j.jconrel.2018.08.010
DO - 10.1016/j.jconrel.2018.08.010
M3 - Article
C2 - 30092254
AN - SCOPUS:85051117283
VL - 286
SP - 315
EP - 325
JO - Journal of Controlled Release
JF - Journal of Controlled Release
SN - 0168-3659
ER -