Evidence map›Paper›PMID 33271859›Full record

ArticlePharmaceutics2020

Semi-Solid Pharmaceutical Formulations for the Delivery of Papain Nanoparticles.

Caroline S A de Lima, Justine P R O Varca, Kamila M Nogueira, Gabriela N Fazolin, Lucas F de Freitas, Eliseu W de Souza, Ademar B Lugão, Gustavo H C Varca

Abstract read
In one paragraph

Article in Pharmaceutics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
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

8 authors.

Caroline S A de LimaNuclear and Energy Research Institute, University of São Paulo, São Paulo 05508-000, Brazil.
Justine P R O VarcaNuclear and Energy Research Institute, University of São Paulo, São Paulo 05508-000, Brazil.
Kamila M NogueiraNuclear and Energy Research Institute, University of São Paulo, São Paulo 05508-000, Brazil.
Gabriela N FazolinNuclear and Energy Research Institute, University of São Paulo, São Paulo 05508-000, Brazil.
Lucas F de FreitasNuclear and Energy Research Institute, University of São Paulo, São Paulo 05508-000, Brazil.
Eliseu W de SouzaDepartment of Polymers, Technology College (Fatec), São Paulo 03694-000, Brazil.
Ademar B LugãoNuclear and Energy Research Institute, University of São Paulo, São Paulo 05508-000, Brazil.
Gustavo H C VarcaNuclear and Energy Research Institute, University of São Paulo, São Paulo 05508-000, Brazil.

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 402887/2013-1Fundação de Amparo à Pesquisa do Estado de São Paulo 2015/13979-0Fundação de Amparo à Pesquisa do Estado de São Paulo 2019/01315-1International Atomic Energy Agency CRPF 22064Sistema Nacional de Laboratórios em Nanotecnologias (SisNano) 442527/2019-5
6 · The paper itself

Abstract

Papain is a therapeutic enzyme with restricted applications due to associated allergenic reactions. Papain nanoparticles have shown to be safe for biomedical use, although a method for proper drug loading and release remains to be developed. Thus, the objective of this work was to develop and assess the stability of papain nanoparticles in a prototype semi-solid formulation suitable for dermatological or topical administrations. Papain nanoparticles of 7.0 ± 0.1 nm were synthesized and loaded into carboxymethylcellulose- and poly(vinyl alcohol)-based gels. The formulations were then assayed for preliminary stability, enzyme activity, cytotoxicity studies, and characterized according to their microstructures and protein distribution. The formulations were suitable for papain nanoparticle loading and provided a stable environment for the nanoparticles. The enzyme distribution along the gel matrix was homogeneous for all the formulations, and the proteolytic activity was preserved after the gel preparation. Both gels presented a slow release of the papain nanoparticles for four days. Cell viability assays revealed no potential cytotoxicity, and the presence of the nanoparticles did not alter the microstructure of the gel. The developed systems presented a potential for biomedical applications, either as drug delivery systems for papain nanoparticles and/or its complexes.

Indexed as

gelnanopapainnanoparticlessemi-solid formulationtherapeutic enzymes

Identifiers

PMID33271859
PMCPMC7761214

What OpenQuestion holds

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Registered trials

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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.