Evidence map›Paper›PMID 37631382›Full record

ArticlePharmaceutics2023

Enhanced Cellular Uptake and Transport of Bovine Lactoferrin Using Pectin- and Chitosan-Modified Solid Lipid Nanoparticles.

Xudong Yao, Craig Bunt, Mengyang Liu, Siew-Young Quek, John Shaw, Jillian Cornish, Jingyuan Wen

Open access · goldAbstract read
In one paragraph

Article in Pharmaceutics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 16% 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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 11 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  6. 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

7 authors at 2 institutions in 1 country.

Xudong YaoSchool of Pharmacy, Faculty of Medical and Health Science, The University of Auckland, Auckland 1142, New Zealand.
Craig BuntDepartment of Food Science, Otago University, Dunedin 9054, New Zealand.
Mengyang LiuSchool of Pharmacy, Faculty of Medical and Health Science, The University of Auckland, Auckland 1142, New Zealand.ORCID 0000-0002-5927-5004
Siew-Young QuekChemical Science, The University of Auckland, Auckland 1142, New Zealand.ORCID 0000-0001-5244-9895
John ShawSchool of Pharmacy, Faculty of Medical and Health Science, The University of Auckland, Auckland 1142, New Zealand.
Jillian CornishSchool of Medicine, Faculty of Medical and Health Science, The University of Auckland, Auckland 1142, New Zealand.
Jingyuan WenSchool of Pharmacy, Faculty of Medical and Health Science, The University of Auckland, Auckland 1142, New Zealand.ORCID 0000-0001-7833-5546
University of Auckland · NZUniversity of Otago · NZ

Funding

Faculty Research Development Fund (FRDF) N/ANew Zealand Pharmacy Education and Research Foundation (NZPERF) N/A
6 · The paper itself

Abstract

aimThe aim of this project is to use pectin- and chitosan-modified solid lipid nanoparticles for bovine lactoferrin to enhance its cellular uptake and transport.

methodsSolid lipid particles containing bovine lactoferrin (bLf) were formulated through the solvent evaporation technique, incorporating stearic acid along with either chitosan or pectin modification. bLf cellular uptake and transport were evaluated in vitro using the human adenocarcinoma cell line Caco-2 cell model. RESULTS AND DISCUSSION: The bLf-loaded SLPs showed no significant effect on cytotoxicity and did not induce apoptosis within the eight-hour investigation. The use of confocal laser scanning microscopy confirmed that bLf follows the receptor-mediated endocytosis, whereas the primary mechanism for the cellular uptake of SLPs was endocytosis. The bLf-loaded SLPs had significantly more cellular uptake compared to bLf alone, and it was observed that this impact varied based on the time, temperature, and concentration. Verapamil and EDTA were determined to raise the apparent permeability coefficients (App) of bLf and bLf-loaded SLPs.

conclusionThis occurred because they hindered efflux by interacting with P-glycoproteins and had a penetration-enhancing influence. These findings propose the possibility of an additional absorption mechanism for SLPs, potentially involving active transportation facilitated by the P-glycoprotein transporter in Caco-2 cells. These results suggest that SLPs have the potential to be applied as effective carriers to improve the oral bioavailability of proteins and peptides.

Indexed as

bovine lactoferrincellular transportcellular uptakechitosan-modified solid lipid nanoparticles

Identifiers

PMID37631382
PMCPMC10457979
OpenAlexW4386027076

What Socratic 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 Socratic graph.