Evidence map›Paper›PMID 30450244›Full record

ArticlePolymers2017

Cellulose Acetate Phthalate and Antiretroviral Nanoparticle Fabrications for HIV Pre-Exposure Prophylaxis.

Subhra Mandal, Karl Khandalavala, Rachel Pham, Patrick Bruck, Marisa Varghese, Andrew Kochvar, Ashley Monaco, Pavan Kumar Prathipati, Christopher Destache, Annemarie Shibata

Open access · goldAbstract read
In one paragraph

Article in Polymers, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.9field-weighted citation impact, top 14% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Novel Antiretroviral Therapeutic Strategies for HIV.Molecules (Basel, Switzerland) · 2021
    Review
  7. Article
  8. Article
  9. Review
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  11. Article
  12. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 1 country.

Subhra MandalSchool of Pharmacy and Health Professions, Creighton University, 2500 California Plaza, Omaha, NE 68178, USA.
Karl KhandalavalaDepartment of Biology, Creighton University, 2500 California Plaza, Omaha, NE 68178, USA.
Rachel PhamDepartment of Biology, Creighton University, 2500 California Plaza, Omaha, NE 68178, USA.
Patrick BruckDana-Farber Cancer Institute, Harvard University, Boston, MA 02215, USA.
Marisa VargheseDepartment of Biology, Creighton University, 2500 California Plaza, Omaha, NE 68178, USA.
Andrew KochvarDepartment of Biology, Creighton University, 2500 California Plaza, Omaha, NE 68178, USA.
Ashley MonacoDepartment of Biology, Creighton University, 2500 California Plaza, Omaha, NE 68178, USA.
Pavan Kumar PrathipatiSchool of Pharmacy and Health Professions, Creighton University, 2500 California Plaza, Omaha, NE 68178, USA.
Christopher DestacheSchool of Pharmacy and Health Professions, Creighton University, 2500 California Plaza, Omaha, NE 68178, USA.
Annemarie ShibataDepartment of Biology, Creighton University, 2500 California Plaza, Omaha, NE 68178, USA.
Creighton University · USHarvard University · US

Funding

Integrase inhibitor combination nanomicrobicide for prevention of HIV infectionR15AI118550 · NIAID · CREIGHTON UNIVERSITY · PI SHIBATA, ANNEMARIE · 2015 to 2015
$437k
NIAID NIH HHS R15 AI118550
6 · The paper itself

Abstract

To adequately reduce new HIV infections, development of highly effective pre-exposure prophylaxis (PrEP) against HIV infection in women is necessary. Cellulose acetate phthalate (CAP) is a pH sensitive polymer with HIV-1 entry inhibitory properties. Dolutegravir (DTG) is an integrase strand transfer inhibitor with potent antiretroviral activity. DTG delivered in combination with CAP may significantly improve current PrEP against HIV. In the present study the development of DTG-loaded CAP nanoparticles incorporated in thermosensitive (TMS) gel at vaginal pH 4.2 and seminal fluid pH 7.4 is presented as proof-of-concept for improved PrEP. Water-oil-in-water homogenization was used to fabricate DTG-loaded CAP nanoparticles (DTG-CAP-NPs). Size, polydispersity, and morphological analyses illustrate that DTG-CAP-NPs were smooth and spherical, ≤200 nm in size, and monodispersed with a polydispersity index PDI ≤ 0.2. The drug encapsulation (EE%) and release profile of DTG-CAP-NPs was determined by HPLC analysis. The EE% of DTG in DTG-CAP-NPs was evaluated to be ∼70%. The thermal sensitivity of the TMS gel was optimized and the pH dependency was evaluated by rheological analysis. DTG release studies in TMS gel revealed that DTG-CAP-NPs were stable in TMS gel at pH 4.2 while DTG-CAP-NPs in TMS gel at pH 7.4 rapidly release DTG (≥80% release within 1 h). Cytotoxicity studies using vaginal cell lines revealed that DTG-CAP-NPs were relatively non-cytotoxic at concentration <1 μg/mL. Confocal microscopic studies illustrate that ≥98% cells retained DTG-CAP-NPs intracellularly over seven days. Antiretroviral drug loaded nanocellulose fabrications in TMS gel delivered intravaginally may enhance both microbicidal and antiretroviral drug efficacy and may present a novel option for female PrEP against HIV.

Indexed as

anti-retroviralcellulose acetate phthalateHIVnanoparticlespre-exposure prophylaxisthermosensitive gel

Identifiers

PMID30450244
PMCPMC6239201
OpenAlexW2751654222

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.