SynthesisDrug design, development and therapy2026
Film-Forming Gels for Topical Drug Delivery: A Systematic Review of the Effects of Formulation on Film Performance, Drug Release, and Skin Permeation.
Synthesis in Drug design, development and therapy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.
What it found
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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.
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.
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Who cites it
4 citing papers in PubMed, 1 synthesis or guideline pooled it.
- Formulation Attributes and Preclinical Wound Healing Outcomes of Natural Product Based Nanoemulsions: A Systematic Review.International journal of nanomedicine · 2026Pooled it
- Review
- Nanomaterials for the Prevention, Detection, and Treatment of Pharyngeal Human Papillomavirus Infection: A Translational Roadmap.Materials (Basel, Switzerland) · 2026Review
- Leciplex Nanocarriers: An Optimized Platform for Thymol Delivery in Acne Management.Pharmaceutics · 2026Article
Corrections and comments
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Authors and funding
9 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Film-forming gels (FFGs) are increasingly recognized as a medium for topical drug delivery. However, existing evidence correlating specific formulation characteristics with drug delivery efficacy remains fragmented across many studies and is only partially organized. This systematic review aimed to consolidate these findings into a single framework and examine how important formulation variables affect three main outcome domains: film characteristics, drug release behavior, and skin permeation. A systematic search of PubMed and Scopus was conducted until October 2025, adhering to the PRISMA criteria. Studies were included if they examined topical FFG formulations and reported at least one of the predetermined outcomes. A total of 27 studies fulfilled the inclusion criteria, with solvent evaporation identified as the predominant method for FFG preparation. Across this body of research, the selection and relative ratio of polymers and plasticizers have consistently emerged as critical determinants influencing drying time (<15 min), mechanical strength, flexibility, and bioadhesive properties of the film on the skin. Most formulations released the drug slowly over approximately 8-48 hours. In studies that measured permeation, FFGs usually exhibited a higher flux and/or better drug retention in the skin than regular topical formulations. The film's ability to block the skin and the use of penetration enhancers in the matrix are thought to cause these effects. In summary, these results show that FFGs are a flexible and customizable formulation platform, where the film's characteristics, release rate, and skin penetration are all strongly linked to the composition's design. To obtain this technology with clearer therapeutic benefits, we need to employ Quality by Design principles more widely and have more consistent evaluation methodologies across studies.
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Registered trials
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.