Evidence map›Paper›PMID 40978372›Full record

ReviewACS omega2025

Advanced Drug Delivery Strategies to Overcome Solubility and Permeability Challenges: Driving Biopharmaceutical Advancements Toward Commercial Success.

Ahmed Raza Hashmi, Mahendran Sekar, Farwa Zahra, Nagashekhara Molugulu, Ling Shing Wong

Abstract readReview
In one paragraph

Review in ACS omega, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. ACS omega · 2026
    Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Review
  8. 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

5 authors.

Ahmed Raza HashmiSchool of Pharmacy, Monash University Malaysia, Bandar Sunway, Subang Jaya, Selangor 47500, Malaysia.
Mahendran SekarSchool of Pharmacy, Monash University Malaysia, Bandar Sunway, Subang Jaya, Selangor 47500, Malaysia.ORCID https://orcid.org/0000-0002-3022-6137
Farwa ZahraSargodha College of Medical Sciences, Lahore - Sargodha Rd, Sargodha 40100, Pakistan.
Nagashekhara MoluguluSchool of Pharmacy, Monash University Malaysia, Bandar Sunway, Subang Jaya, Selangor 47500, Malaysia.
Ling Shing WongFaculty of Health and Life Sciences, INTI International University, Nilai 71800, Malaysia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oral drug administration is the safest and most convenient route for drug delivery. Nevertheless, solubility and permeability are two major issues regarding drug design; these issues must be addressed to overcome the biopharmaceutical challenges associated with them. Drugs are classified into four groups according to the biopharmaceutical classification system. Furthermore, drugs from BCS class II demonstrate poor solubility; meanwhile, drugs related to BCS class IV show poor solubility along with poor permeability. However, some drugs of BCS class IV are also substrates for p-glycoprotein and CYP3A4. These features lead to issues of bioavailability and reduced patient compliance. Moreover, the anatomical and physiological behavior of the body and physicochemical features of the drug are also associated with compromised bioavailability. All these concerns make it difficult for any formulator to manufacture drugs, and hurdles related to these drugs make it difficult to deliver them to the actual market. Hence, this review aims to summarize the advanced innovative methodologies to get suitable solutions to overcome the limitations associated with solubility and permeability and accordingly improve the drug's bioavailability. Traditional approaches like physical modifications of drugs, i.e., micronization, solid dispersion in carriers, complexation, cryogenic techniques, and supercritical fluid technology; moreover, chemical modifications of drugs, i.e., salt formation, cosolvency, hydrotropy, and prodrug formation, contribute to treating solubility problems. Meanwhile, a few advanced drug delivery strategies, including lipid-based drug delivery systems, polymeric nanocarriers, pharmaceutically engineered crystals, and p-gp efflux pump inhibitors, have been mentioned that aid in improving the drug's stability in diverse bodily environment, enhance solubility along with permeability, and increasing bioavailability, which directly leads to enhanced patient compliance. Incorporating these methods is essential to address solubility and permeability challenges, lower treatment costs, and enhance patient outcomes. Nanobased delivery systems offer significant potential for improving therapeutic effectiveness and patient compliance.

Identifiers

PMID40978372
PMCPMC12444610

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.