PolySciTech (www.polyscitech.com) provides a wide
array of PEG-PLA polymers. Recently this type of polymer was utilized to
generate nanoparticles encapsulating DAAN15h. a potent reverse transcriptase
inhibitor, to improve blood circulation time and reduce elimination. Read more:
Li, Wen, Qian Wang, Yuan Li, Fei Yu, Qi Liu, Bingjie Qin, Lan Xie, Lu Lu, and
Shibo Jiang. "A Nanoparticle-Encapsulated Non-Nucleoside
Reverse-Transcriptase Inhibitor with Enhanced Anti-HIV-1 Activity and Prolonged
Circulation Time in Plasma." Current pharmaceutical design 21, no. 7
(2015): 925-935.
http://www.ingentaconnect.com/content/ben/cpd/2015/00000021/00000007/art00011
“Abstract:
Non-nucleoside reverse-transcriptase inhibitors (NNRTIs), major components of
highly active antiretroviral therapy (HAART), are effective in suppressing
viral replication and preventing the progress of HIV-1 infection to AIDS.
However, rapid blood clearance in vivo could significantly impair the
efficiency of the anti-HIV-1 activity and result in multiple daily doses which
might lead to poor patient compliance. Here we attempted to employ
biodegradable organic nanoparticles (NPs) to encapsulate DAAN15h, a derivative
of 4-substituted 1, 5-diarylaniline with potent anti-HIV activities.
Nanoparticles encapsulating DAAN15h (NP-DAAN15h) displayed a spherical shape
with a size of 97.01 ± 3.64 nm and zeta potential of -19.1 ± 3.78 mV, and they
exhibited a sustained controlled release behavior in vitro. The cellular uptake
of NPs on TZM-b1 cells, MT-2 cells and M7 cells, possibly through lipid
raft-mediated and energydependent active transport processes, was significantly
enhanced. NP-DAAN15h, which possessed no significant in vitro cytotoxicity,
showed improved antiviral activity against laboratory-adapted and primary HIV-1
isolates with different subtypes and tropisms, including RT-resistant variants.
NP-DAAN15h exhibited a significantly prolonged blood circulation time,
decreased plasma elimination rate, and enhanced AUC(0-t). NP-DAAN15h, a
nanoparticle-encapsulated NNRTI, exhibits enhanced cellular uptake, improved
anti-HIV-1 efficacy and prolonged in vivo circulation time, suggesting good
potential for further development as a new NNRTI formulation for clinical use. Keywords:
HIV-1; antiretroviral therapy; drug resistance; nanoparticles; non-nucleoside
reverse-transcriptase inhibitor; pharmacokinetics”
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