Evidence map›Paper›PMID 28243062›Full record

ReviewDrug design, development and therapy2017

Oral and transdermal drug delivery systems: role of lipid-based lyotropic liquid crystals.

Rajan Rajabalaya, Muhammad Nuh Musa, Nurolaini Kifli, Sheba R David

Abstract readReview
In one paragraph

Review in Drug design, development and therapy, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing 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

30 citing papers in PubMed.

  1. Article
  2. Liquid crystalline system for drug delivery: structural insights, preparation techniques and translational potential.Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2026
    Review
  3. Review
  4. Review
  5. Article
  6. Synthesis and Self-Assembly of Poly(4-acetoxystyrene) Cubosomes.Macromolecular rapid communications · 2025
    Article
  7. Review
  8. Review
  9. Article
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  11. Article
  12. Article
  13. Article
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  15. Article
  16. Article
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  19. Review
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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

4 authors.

Rajan RajabalayaPAPRSB Institute of Health Sciences, Universiti Brunei Darussalam, Brunei Darussalam.
Muhammad Nuh MusaPAPRSB Institute of Health Sciences, Universiti Brunei Darussalam, Brunei Darussalam.
Nurolaini KifliPAPRSB Institute of Health Sciences, Universiti Brunei Darussalam, Brunei Darussalam.
Sheba R DavidPAPRSB Institute of Health Sciences, Universiti Brunei Darussalam, Brunei Darussalam.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Liquid crystal (LC) dosage forms, particularly those using lipid-based lyotropic LCs (LLCs), have generated considerable interest as potential drug delivery systems. LCs have the physical properties of liquids but retain some of the structural characteristics of crystalline solids. They are compatible with hydrophobic and hydrophilic compounds of many different classes and can protect even biologicals and nucleic acids from degradation. This review, focused on research conducted over the past 5 years, discusses the structural evaluation of LCs and their effects in drug formulations. The structural classification of LLCs into lamellar, hexagonal and micellar cubic phases is described. The structures of these phases are influenced by the addition of surfactants, which include a variety of nontoxic, biodegradable lipids; these also enhance drug solubility. LLC structure influences drug localization, particle size and viscosity, which, in turn, determine drug delivery properties. Through several specific examples, we describe the applications of LLCs in oral and topical drug formulations, the latter including transdermal and ocular delivery. In oral LLC formulations, micelle compositions and the resulting LLC structures can determine drug solubilization and stability as well as intestinal transport and absorption. Similarly, in topical LLC formulations, composition can influence whether the drug is retained in the skin or delivered transdermally. Owing to their enhancement of drug stability and promotion of controlled drug delivery, LLCs are becoming increasingly popular in pharmaceutical formulations.

Indexed as

Administration, CutaneousAdministration, OralAnimalsDrug CompoundingDrug Delivery SystemsHumansHydrophobic and Hydrophilic InteractionsLipidsLiquid CrystalsLipidscontrolled releasedrug deliverydrug localizationliquid crystallyotropicsurfactants

Identifiers

PMID28243062
PMCPMC5315216

What OpenQuestion holds

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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.