Evidence map›Paper›PMID 41138888›Full record

ArticleInternational journal of pharmaceutics2025

Binary lipid system-based granules with undissolved drug crystals enhance oral bioavailability by preventing degradation and improving permeability.

Xiaowei Dong, Tao Zhang, Liangqiao Bian

Abstract read
In one paragraph

Article in International journal of pharmaceutics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

3 authors.

Xiaowei DongDepartment of Pharmaceutical Sciences, University of North Texas Health Science Center, Fort Worth, TX, USA. Electronic address: xiaowei.dong@unthsc.edu.
Tao ZhangDepartment of Pharmaceutical Sciences, SUNY-Binghamton University, Binghamton, NY, USA.
Liangqiao BianShimadzu Center for Advanced Analytical Chemistry, University of Texas at Arlington, Arlington, TX, USA.

Funding

Research Supplements for R35 to Promote Diversity in Health-Related Research, PA-21-071R35GM138225 · NIGMS · UNIVERSITY OF NORTH TEXAS HLTH SCI CTR · PI DONG, XIAOWEI · 2020 to 2025
$2.1M
NIGMS NIH HHS R35 GM138225
6 · The paper itself

Abstract

Conventional oral drug delivery systems, such as lipid-based formulations and nanoparticles, require drugs to fully dissolve in excipients to improve solubility and bioavailability. However, many drugs, including olmesartan medoxomil (OLM), an ester prodrug for hypertension, have low solubility in water, lipids, and surfactants, resulting in low drug loading (e.g. 1 ∼ 2 % drug loading) and formulation challenges. Premature degradation of ester prodrugs is also a major factor contributing to the low bioavailability of prodrugs. This study developed OLM lipid-solid granules (LSG) by coating OLM crystals with a binary lipid system (BLS) composed of one lipid and one water-soluble surfactant only. The OLM granules achieved 10 % drug loading and increased relative bioavailability to 625 %, surpassing all previously reported formulations containing dissolved OLM. Extensive in vitro studies, including two-step dissolution and Caco-2 cell assays with and without esterase, demonstrated that OLM LSG protected OLM from esterase-mediated hydrolysis and enhanced drug uptake and permeability. Pharmacokinetics and tissue distribution confirmed enhanced small intestine absorption. This novel approach introduces a transformative concept of coating drug crystals with a BLS in solid granules to enhance oral absorption and eliminates the need to dissolve drugs in excipients. It represents a fundamental shift in the use of lipids and surfactants, offering a promising platform for delivering prodrugs with low solubility and susceptibility to hydrolysis.

Indexed as

LipidsAdministration, OralAnimalsBiological AvailabilityCaco-2 CellsCrystallizationDrug Delivery SystemsExcipientsHumansHydrolysisIntestinal AbsorptionMalePermeabilityProdrugsRatsRats, Sprague-DawleyExcipientsLipidsProdrugsSurface-Active AgentsDrug degradationDrug solid granulesLipid and surfactantOral absorption enhancementProdrugsWater-insoluble drugs

Identifiers

PMID41138888
PMCPMC13182864

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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.