2016
DOI: 10.1016/j.jconrel.2016.09.020
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Nanoparticles-in-film for the combined vaginal delivery of anti-HIV microbicide drugs

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Cited by 88 publications
(66 citation statements)
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“…A few studies detailing on NPs in films as potential microbicide products have been described (Table 1.2.2). [128][129][130][131] For example, our group demonstrated the versatility and potential usefulness of NPs-in-film systems for delivering a combination of hydrophobic (efavirenz) and hydrophilic (tenofovir) antiretroviral drugs. 131 Efavirenz-loaded PLGA NPs and tenofovir were incorporated into the polymer matrix during manufacturing by solvent casting.…”
Section: Delivery Platforms For Nanomicrobicidesmentioning
confidence: 99%
See 1 more Smart Citation
“…A few studies detailing on NPs in films as potential microbicide products have been described (Table 1.2.2). [128][129][130][131] For example, our group demonstrated the versatility and potential usefulness of NPs-in-film systems for delivering a combination of hydrophobic (efavirenz) and hydrophilic (tenofovir) antiretroviral drugs. 131 Efavirenz-loaded PLGA NPs and tenofovir were incorporated into the polymer matrix during manufacturing by solvent casting.…”
Section: Delivery Platforms For Nanomicrobicidesmentioning
confidence: 99%
“…Furthermore, NPs were found to deeply penetrate the mucosa and reach the stroma. 131 PK of efavirenz in vaginal tissue and lavage were improved when the drug was associated with NPs: relative bioavailability in tissue and lavage was increased by roughly 2 and 6 times, respectively, as compared to films containing free efavirenz (i.e., directly dispersed in the film matrix without the incorporation of NPs). All drug assays were performed using a validated liquid chromatography-tandem mass spectrometry method.…”
Section: Delivery Platforms For Nanomicrobicidesmentioning
confidence: 99%
“…The advantages of nanoparticles combine with the benefits of the films described above; examples of this are PVA films incorporating nanoparticles loaded with small interfering RNA 203. The incorporation of nanoparticles loaded with TFV or efavirenz into a film based on HPMC, PVA and glycerine was also evaluated,204 and was found to produce sustained release of the drug for 24 hours and was found to be safe at in vivo trials 205. Finally, it is worth mentioning another similar case in which PLGA nanoparticles were loaded with another antiretroviral, IQP-0528, and incorporated into a fast-dissolving film 206…”
Section: The Future Of Microbicidesmentioning
confidence: 99%
“…Dosing amount and restrictions on dosage size could be a limitation for film dosage forms. A wide array of physicochemically diverse ARV drugs have been incorporated into films namely TFV [73, 70], DPV [17, 73, 108], EfdA [109], efavirenz [110], RC-101 [77], VRC01 anti-HIV mAb [111], and si-RNA and nanoparticles [112]. …”
Section: On-demand Vaginal Rectal and Dual Compartment Dosage Formsmentioning
confidence: 99%
“…These nanolipogels contain nanoparticles with a hydrogel-core and lipid-shell. Additionally, nanoparticles have been combined with traditional dosage forms such as gels [93] and films [110]. One of these platforms, VivaGel ™ , which is a dendrimer-based gel, has shown acceptability and high activity against HIV-1 and HSV-2 in human studies [124].…”
Section: On-demand Vaginal Rectal and Dual Compartment Dosage Formsmentioning
confidence: 99%