Evidence map›Paper›PMID 40531754›Full record

ReviewBrazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica2025

Nanoparticle tools for maximizing oral drug delivery.

D M Cahyani, A S Mubarok, B S Hariawan, I Amalina, P Drake, T Parumasivam, R K Sahu, M A S Rijal, R Sari, A Miatmoko

Abstract readReview
In one paragraph

Review in Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Natural Products with Pharmaceutical Activities.Molecules (Basel, Switzerland) · 2025
    Article
  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

10 authors.

D M CahyaniMaster Program of Pharmaceutical Sciences, Faculty of Pharmacy, Universitas Airlangga, Campus C UNAIR Mulyorejo, Surabaya, Indonesia.ORCID http://orcid.org/0000-0002-1254-9274
A S MubarokMaster Program of Pharmaceutical Sciences, Faculty of Pharmacy, Universitas Airlangga, Campus C UNAIR Mulyorejo, Surabaya, Indonesia.ORCID http://orcid.org/0009-0009-3418-8738
B S HariawanMaster Program of Pharmaceutical Sciences, Faculty of Pharmacy, Universitas Airlangga, Campus C UNAIR Mulyorejo, Surabaya, Indonesia.ORCID http://orcid.org/0000-0002-0109-6206
I AmalinaNanotechnology Engineering, Faculty of Advanced Technology and Multidiscipline, Universitas Airlangga, Campus C UNAIR Mulyorejo, Surabaya, Indonesia.ORCID http://orcid.org/0000-0001-9578-6680
P DrakeSchool of Chemistry and Biosciences, Faculty of Life Sciences, University of Bradford, Bradford, UK.ORCID http://orcid.org/0000-0002-0536-4378
T ParumasivamSchool of Pharmaceutical Sciences, Universiti Sains Malaysia, Pulau Pinang, Malaysia.ORCID http://orcid.org/0000-0001-6278-3627
R K SahuDepartment of Pharmaceutical Sciences, Hemvati Nandan Bahuguna Garhwal University (A Central University), Chauras Campus, Tehri Garhwal, Uttarakhand, India.ORCID http://orcid.org/0000-0001-5671-6591
M A S RijalDepartment of Pharmaceutical Sciences, Faculty of Pharmacy, Universitas Airlangga, Campus C UNAIR Mulyorejo, Surabaya, Indonesia.ORCID http://orcid.org/0000-0001-6881-1684
R SariDepartment of Pharmaceutical Sciences, Faculty of Pharmacy, Universitas Airlangga, Campus C UNAIR Mulyorejo, Surabaya, Indonesia.ORCID http://orcid.org/0000-0002-3391-1877
A MiatmokoDepartment of Pharmaceutical Sciences, Faculty of Pharmacy, Universitas Airlangga, Campus C UNAIR Mulyorejo, Surabaya, Indonesia.ORCID http://orcid.org/0000-0003-1658-0778

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The biological permeability and water solubility of drugs can pose substantial obstacles to oral drug delivery, the most common mode of drug administration for improving human health. Solubility determines the amount of drug that can be dissolved in solution, whereas permeability is the ability to permeate across biological membranes, determining therapeutic efficacy and safety. Some biological barriers, such as gastrointestinal pH, enzymes, and mucus, may affect the dissolution or absorption of therapeutic drugs. Physical or chemical approaches can be used to modify the water solubility or enhance the permeability. Moreover, nanocarriers, which can increase drug stability through encapsulation, enhance absorption due to their extensive surface area, and facilitate the targeted administration of medications to certain areas, could be useful for drug delivery systems. Nanoparticles can increase drug solubility by particle size reduction, complexation, and drug encapsulation and increase permeation by retention in tumors, opening of tight junctions, membrane fluidization, or intestinal mucoadhesion. Despite the many advantages of nanoparticle drug formulations, they also have several limitations, such as complicated manufacturing processes, nanotoxicity, and stability issues. In this article, we provide a comprehensive description of nanoparticle tools for maximizing oral drug delivery.

Indexed as

Drug Delivery SystemsNanoparticle Drug Delivery SystemNanoparticlesAdministration, OralHumansParticle SizePermeabilitySolubilityNanoparticle Drug Delivery System

Identifiers

PMID40531754
PMCPMC12172155

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.