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Polyvinyl Alcohol

Drugs and Chemicals · NLM MeSH · updated 2026-10-31 · version 1

Citations verified against PubMedNot yet clinician-reviewed10 referencesApproximately 4 min read

A polymer prepared from polyvinyl acetates by replacement of the acetate groups with hydroxyl groups.

Table of Contents

1. Definition2. Research landscape3. Reading the evidence4. Open-access studies5. Key reviews6. References7. About this article

Definition and research guide

This page combines a MeSH definition, publication statistics and selected research abstracts. It is a starting point for reading the literature, not a medical textbook or a systematic evidence review.

Content available: 4 complete abstracts (670 words), 10 references. Full article text is not stored or reproduced here; follow the PMID, DOI or PMC links to read the original sources and their access terms.

Definition

A polymer prepared from polyvinyl acetates by replacement of the acetate groups with hydroxyl groups. It is used as a pharmaceutic aid and ophthalmic lubricant as well as in the manufacture of surface coatings artificial sponges, cosmetics, and other products.

Definition: NLM Medical Subject Headings (MeSH) scope note (Public domain (U.S. National Library of Medicine); attribution requested). View the MeSH record.

Also known as: Alcohol, Polyvinyl; Polyviol; Liquifilm Tears; Tears, Liquifilm.

Where it fits in the MeSH classification

Broader topics
Alcohols; Polyvinyls

Research landscape

PubMed indexes 8,398 records tagged with the MeSH heading “Polyvinyl Alcohol” (counts retrieved 2026-10-31). 3,567 of them (42.5%) were published from 2020 onward, and the busiest period so far is 2020 onward with 3,567 records.

Reviews account for 145 records (1.7%) and meta-analyses for 9. Randomized controlled trials number 111 (1.3%) as a share of all records on the topic. Randomized trials make up only a small share of this literature, so much of what is known comes from laboratory, observational or descriptive work.

PubMed records by publication periodthrough 1999: 976 records; 2000-2009: 1,244 records; 2010-2019: 2,611 records; 2020 onward: 3,567 records976through 19991,2442000-20092,6112010-20193,5672020 onward
Records in PubMed indexed with this heading, by publication period. Real counts from NCBI E-utilities; the final period covers only part of the current year. Volume reflects how much has been published, not how strong the evidence is.
Show the data
PeriodRecords
through 1999976
2000-20091,244
2010-20192,611
2020 onward3,567
Share of records by publication typeReviews: 1.7 percent; Meta-analyses: 0.1 percent; Randomized controlled trials: 1.3 percentReviews1.7% (145)Meta-analyses0.1% (9)Randomized controlled trials1.3% (111)
Share of all PubMed records on this heading that carry each publication type. Types overlap with other records, so the shares do not sum to 100%.
Publication-type chart data
Publication types among 8,398 PubMed records
TypeRecordsShare
Reviews1451.7%
Meta-analyses90.1%
Randomized controlled trials1111.3%

Method: PubMed query "Polyvinyl Alcohol"[MeSH Terms] with publication-type and date filters, retrieved 2026-10-31.

Reading the evidence in drugs and chemicals

Studies of a chemical or drug can answer very different questions: what it is and how it behaves in cells and animals, how the body handles it, and whether it changes outcomes in people. Laboratory and animal findings often do not carry over to patients, and observational studies of exposures are confounded by who uses a substance and why. Nothing on this page is a recommendation to use, avoid, start or stop any substance or medicine; talk to a qualified clinician or pharmacist about your own situation. Check the dose, the species, the comparison group and whether a patient-relevant outcome was measured.

Evidence from open-access studies

These open-access studies come from PubMed’s best-match results for this heading (papers whose main topic it is), ranked here by citation count, with one recent addition. Each abstract is reproduced in full under its recorded open licence so that you can read the authors’ own words. They illustrate the literature; they are not a systematic summary of it. Citation counts measure attention, not reliability or clinical benefit.

Study comparison — selected abstracts, not a systematic review
Study / authorsYearSource label / designEurope PMC citationsLicence / source
Bio-inspired sensitive and reversible mechanochromisms via strain-dependent cracks and folds
Zeng S, Zhang D, Huang W, Wang Z, Freire SG, Yu X, et al.
2016Research article
Design not recorded in structured metadata
114cc by
PMID 27389480 · DOI · PMC4941047
Hemostatic and antibacterial PVA/Kaolin composite sponges loaded with penicillin-streptomycin for wound dressing applications
Tamer TM, Sabet MM, Omer AM, Abbas E, Eid AI, Mohy-Eldin MS, et al.
2021Research article
Design not recorded in structured metadata
79cc by
PMID 33564036 · DOI · PMC7873205
Conducting molybdenum sulfide/graphene oxide/polyvinyl alcohol nanocomposite hydrogel for repairing spinal cord injury
Chen L, Wang W, Lin Z, Lu Y, Chen H, Li B, et al.
2022Research article
Design not recorded in structured metadata
58cc by
PMID 35524268 · DOI · PMC9074236
Sulfate resistance of polyvinyl alcohol and basalt fibers reinforced red mud concrete
Xu F, Liu A, Liu Z, Fang Z
2026Research article
Design not recorded in structured metadata
0cc by
PMID 42726737 · DOI · PMC13567797

Bio-inspired sensitive and reversible mechanochromisms via strain-dependent cracks and folds [1]

Research article Zeng S, Zhang D, Huang W, Wang Z, Freire SG, Yu X, et al. · · 2016 · cited 114 times (Europe PMC)

Abstract reading summary — source excerpts
Opening excerpt
A number of marine organisms use muscle-controlled surface structures to achieve rapid changes in colour and transparency with outstanding reversibility.
Closing excerpt
The EM device can reversibly reveal and conceal any desirable patterns.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (135 words)

A number of marine organisms use muscle-controlled surface structures to achieve rapid changes in colour and transparency with outstanding reversibility. Inspired by these display tactics, we develop analogous deformation-controlled surface-engineering approaches via strain-dependent cracks and folds to realize the following four mechanochromic devices: (1) transparency change mechanochromism (TCM), (2) luminescent mechanochromism (LM), (3) colour alteration mechanochromism (CAM) and (4) encryption mechanochromism (EM). These devices are based on a simple bilayer system that exhibits a broad range of mechanochromic behaviours with high sensitivity and reversibility. The TCM device can reversibly switch between transparent and opaque states. The LM can emit intensive fluorescence as stretched with very high strain sensitivity. The CAM can turn fluorescence from green to yellow to orange as stretched within 20% strain. The EM device can reversibly reveal and conceal any desirable patterns.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 27389480 · DOI · PMC4941047

Hemostatic and antibacterial PVA/Kaolin composite sponges loaded with penicillin-streptomycin for wound dressing applications [2]

Research article Tamer TM, Sabet MM, Omer AM, Abbas E, Eid AI, Mohy-Eldin MS, et al. · · 2021 · cited 79 times (Europe PMC)

Abstract reading summary — source excerpts
Opening excerpt
Hemorrhage is the major hindrance over the wound healing, which triggers microbial infections and might provoke traumatic death.
Closing excerpt
1 sponge could be applied as a multifunctional wound dressing.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (211 words)

Hemorrhage is the major hindrance over the wound healing, which triggers microbial infections and might provoke traumatic death. Herein, new hemostatic and antibacterial PVA/Kaolin composite sponges were crosslinked using a freeze-thawing approach and boosted by penicillin-streptomycin (Pen-Strep). Physicochemical characteristics of developed membranes were analyzed adopting Fourier transformed infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), a thermal gravimetric analyzer (TGA), and differential scanning calorimetry (DSC). Furthermore, the impacts of kaolin concentrations on porosity, swelling behavior, gel fraction, and degradation of the membranes were investigated. SEM analyses revealed a spongy-like structure of hydrogels associated with high dispersion of kaolin inside PVA matrix. The thermal characteristics of PVA/Kaolin were significantly ameliorated compared to the prime PVA. Moreover, the results exhibited significant variations of swelling performance, surface roughness and pore capacity due to the alterations of kaolin contents. Besides, the adhesive strength ability was manifestly enhanced for PVA-K0.1 sponge. Biomedical evaluations including antibacterial activity, blood clotting index and thrombogenicity of the membranes were studied. The contact of PVA/Kaolin to blood revealed notable augmentation in blood clotting. Furthermore, the incorporation of kaolin into PVA presented mild diminution in antibacterial activities. Moreover, PVA/Kaolin composites illustrated no cellular toxicity towards fibroblast cells. These remarkable features substantiate that the PVA-K0.1 sponge could be applied as a multifunctional wound dressing.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 33564036 · DOI · PMC7873205

Conducting molybdenum sulfide/graphene oxide/polyvinyl alcohol nanocomposite hydrogel for repairing spinal cord injury [3]

Research article Chen L, Wang W, Lin Z, Lu Y, Chen H, Li B, et al. · · 2022 · cited 58 times (Europe PMC)

Abstract reading summary — source excerpts
Opening excerpt
A sort of composite hydrogel with good biocompatibility, suppleness, high conductivity, and anti-inflammatory activity based on polyvinyl alcohol (PVA) and molybdenum sulfide/graphene oxide (MoS2/GO) nanomaterial has been developed for spinal cord injury (SCI) restoration.
Closing excerpt
Overall, our work provides a new sort of hydrogels for SCI reparation, which shows great promise for improving the dilemma in SCI therapy.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (137 words)

A sort of composite hydrogel with good biocompatibility, suppleness, high conductivity, and anti-inflammatory activity based on polyvinyl alcohol (PVA) and molybdenum sulfide/graphene oxide (MoS2/GO) nanomaterial has been developed for spinal cord injury (SCI) restoration. The developed (MoS2/GO/PVA) hydrogel exhibits excellent mechanical properties, outstanding electronic conductivity, and inflammation attenuation activity. It can promote neural stem cells into neurons differentiation as well as inhibit the astrocytes development in vitro. In addition, the composite hydrogel shows a high anti-inflammatory effect. After implantation of the composite hydrogel in mice, it could activate the endogenous regeneration of the spinal cord and inhibit the activation of glial cells in the injured area, thus resulting in the recovery of locomotor function. Overall, our work provides a new sort of hydrogels for SCI reparation, which shows great promise for improving the dilemma in SCI therapy.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 35524268 · DOI · PMC9074236

Sulfate resistance of polyvinyl alcohol and basalt fibers reinforced red mud concrete [4]

Research article Xu F, Liu A, Liu Z, Fang Z · · 2026

Abstract reading summary — source excerpts
Opening excerpt
The present study investigated the reinforcement effects of polyvinyl alcohol fiber (PVAF) and basalt fiber (BF) on the performance of fiber reinforced red mud concrete (FRMC) under sulfate drying-wetting cycle.
Closing excerpt
Meanwhile, the synergistic effect of the fibers delayed the degradation of C-S-H gel, thereby effectively improving the sulfate resistance of FRMC.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (187 words)

The present study investigated the reinforcement effects of polyvinyl alcohol fiber (PVAF) and basalt fiber (BF) on the performance of fiber reinforced red mud concrete (FRMC) under sulfate drying-wetting cycle. The underlying mechanisms were further explored through macroscopic performance tests in combination with pore structure, micro-morphology, and phase composition analyses. The results showed that incorporation of BF exhibited a more pronounced improvement in the sulfate resistance of FRMC compared to PVAF. Additionally, FRMC with hybrid PVAF of 0.15% and BF of 0.1% had higher sulfate resistance coefficient (0.854) after 60 cycles, showing the optimal resistance to sulfate attack. The microstructural observations showed that fibers effectively delayed the initiation and propagation of cracks under sulfate drying-wetting cycles. Thus, the fibers provided space for the accumulation of corrosion products, continuously increasing the mass of FRMC, and maintaining overall structural integrity. Pore structure analysis indicated that an appropriate amount of hybrid fibers optimized the pore structure, reducing the porosity and average pore diameter to 20.30% and 26.80 nm, respectively. Meanwhile, the synergistic effect of the fibers delayed the degradation of C-S-H gel, thereby effectively improving the sulfate resistance of FRMC.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 42726737 · DOI · PMC13567797

Key reviews and meta-analyses

The most cited review-type papers among PubMed’s best-match results for this heading, listed with bibliographic details only. Follow the links for the full text and access terms.

  • Research article A review of polyvinyl alcohol and its uses in cartilage and orthopedic applications [5]
    Baker MI, Walsh SP, Schwartz Z, Boyan BD · J Biomed Mater Res B Appl Biomater · 2012 · cited 400 times (Europe PMC)
  • Research article Review of the oral toxicity of polyvinyl alcohol (PVA) [6]
    DeMerlis CC, Schoneker DR · Food Chem Toxicol · 2003 · cited 334 times (Europe PMC)
  • Research article Biomaterials of PVA and PVP in medical and pharmaceutical applications: Perspectives and challenges [7]
    Teodorescu M, Bercea M, Morariu S · Biotechnol Adv · 2019 · cited 248 times (Europe PMC)
  • Research article Properties and Applications of Polyvinyl Alcohol, Halloysite Nanotubes and Their Nanocomposites [8]
    Gaaz TS, Sulong AB, Akhtar MN, Kadhum AA, Mohamad AB, Al-Amiery AA · Molecules · 2015 · cited 223 times (Europe PMC)
  • Research article Monoliths for fast bioseparation and bioconversion and their applications in biotechnology [9]
    Jungbauer A, Hahn R · J Sep Sci · 2004 · cited 110 times (Europe PMC)
  • Research article Recent advances in PVA-polysaccharide based hydrogels and electrospun nanofibers in biomedical applications: A review [10]
    Kamoun EA, Loutfy SA, Hussein Y, Kenawy ES · Int J Biol Macromol · 2021 · cited 104 times (Europe PMC)

References

  1. Zeng S, Zhang D, Huang W, Wang Z, Freire SG, Yu X, et al.. Bio-inspired sensitive and reversible mechanochromisms via strain-dependent cracks and folds. . 2016. PMID 27389480 · DOI · PMC4941047
  2. Tamer TM, Sabet MM, Omer AM, Abbas E, Eid AI, Mohy-Eldin MS, et al.. Hemostatic and antibacterial PVA/Kaolin composite sponges loaded with penicillin-streptomycin for wound dressing applications. . 2021. PMID 33564036 · DOI · PMC7873205
  3. Chen L, Wang W, Lin Z, Lu Y, Chen H, Li B, et al.. Conducting molybdenum sulfide/graphene oxide/polyvinyl alcohol nanocomposite hydrogel for repairing spinal cord injury. . 2022. PMID 35524268 · DOI · PMC9074236
  4. Xu F, Liu A, Liu Z, Fang Z. Sulfate resistance of polyvinyl alcohol and basalt fibers reinforced red mud concrete. . 2026. PMID 42726737 · DOI · PMC13567797
  5. Baker MI, Walsh SP, Schwartz Z, Boyan BD. A review of polyvinyl alcohol and its uses in cartilage and orthopedic applications. J Biomed Mater Res B Appl Biomater. 2012. PMID 22514196 · DOI
  6. DeMerlis CC, Schoneker DR. Review of the oral toxicity of polyvinyl alcohol (PVA). Food Chem Toxicol. 2003. PMID 12504164 · DOI
  7. Teodorescu M, Bercea M, Morariu S. Biomaterials of PVA and PVP in medical and pharmaceutical applications: Perspectives and challenges. Biotechnol Adv. 2019. PMID 30472307 · DOI
  8. Gaaz TS, Sulong AB, Akhtar MN, Kadhum AA, Mohamad AB, Al-Amiery AA. Properties and Applications of Polyvinyl Alcohol, Halloysite Nanotubes and Their Nanocomposites. Molecules. 2015. PMID 26703542 · DOI · PMC6332455
  9. Jungbauer A, Hahn R. Monoliths for fast bioseparation and bioconversion and their applications in biotechnology. J Sep Sci. 2004. PMID 15354554 · DOI
  10. Kamoun EA, Loutfy SA, Hussein Y, Kenawy ES. Recent advances in PVA-polysaccharide based hydrogels and electrospun nanofibers in biomedical applications: A review. Int J Biol Macromol. 2021. PMID 34358597 · DOI

About this article

Sources
NLM Medical Subject Headings (definition, synonyms); NCBI PubMed (counts, identifiers); Europe PMC (open-access abstracts and citation counts).
Verification
Every reference was resolved against PubMed on 2026-10-31; title, year and DOI matched.
Review state
automated source verified; no human expert review has been recorded yet.
Version
1, last updated 2026-10-31.

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At a glance

8,398
PubMed records on this heading
42%
published since 2020
145
review articles
111
randomized trials
10
verified references below

Counts come from PubMed on 2026-10-31; they show how much has been written, not how strong the evidence is.

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