Polyvinylpyrrolidone

Polyvinylpyrrolidone
Names
IUPAC name
1-ethenylpyrrolidin-2-one
Other names
PVP, Povidone, Copovidone

PVPP, Crospovidone, Polyvidone
PNVP
Poly[1-(2-oxo-1-pyrrolidinyl)ethylen]
1-Ethenyl-2-pyrrolidon homopolymer

1-Vinyl-2-pyrrolidinon-Polymere
Identifiers
3D model (JSmol)
Abbreviations PVP, PVPP, NVP, PNVP
ChemSpider
  • none
ECHA InfoCard 100.111.937
E number E1201 (additional chemicals)
Properties
(C6H9NO)n
Molar mass 2.500 – 2.500.000 g·mol−1
Appearance white to light yellow, hygroscopic, amorphous powder
Density 1.2 g/cm3
Melting point 150 to 180 °C (302 to 356 °F; 423 to 453 K) (glass temperature)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Polyvinylpyrrolidone (PVP), also commonly called polyvidone or povidone, is a water-soluble polymer made from the monomer N-vinylpyrrolidone:[1]

Uses

Medical

PVP was used as a plasma volume expander for trauma victims after the 1950s.

It is used as a binder in many pharmaceutical tablets;[2] it simply passes through the body when taken orally. However, autopsies have found that crospovidone (PVPP) contributes to pulmonary vascular injury in substance abusers who have injected pharmaceutical tablets intended for oral consumption.[3] The long-term effects of crospovidone or povidone within the lung are unknown. PVP added to iodine forms a complex called povidone-iodine that possesses disinfectant properties.[4] This complex is used in various products like solutions, ointment, pessaries, liquid soaps and surgical scrubs. It is known under the trade names Pyodine and Betadine among a plethora of others.

It is used in pleurodesis (fusion of the pleura because of incessant pleural effusions). For this purpose, povidone iodine is equally effective and safe as talc, and may be preferred because of easy availability and low cost.[5]

Povidone is used as a lubricant in some eye drops, e.g. Bausch & Lomb's Soothe.

Technical

PVP is also used in many technical applications:

Other uses

PVP binds to polar molecules exceptionally well, owing to its polarity. This has led to its application in coatings for photo-quality ink-jet papers and transparencies, as well as in inks for inkjet printers.

PVP is also used in personal care products, such as shampoos and toothpastes, in paints, and adhesives that must be moistened, such as old-style postage stamps and envelopes. It has also been used in contact lens solutions and in steel-quenching solutions.[9][10] PVP is the basis of the early formulas for hair sprays and hair gels, and still continues to be a component of some.

As a food additive, PVP is a stabilizer and has E number E1201. PVPP (crospovidone) is E1202. It is also used in the wine industry as a fining agent for white wine or some beers. Other references state that polyvinyl pyrrolidone and its derivatives are fully from mineral synthetic origin. Therefore, its use in the production should not be a problem for vegans.

In molecular biology, PVP can be used as a blocking agent during Southern blot analysis as a component of Denhardt's buffer. It is also exceptionally good at absorbing polyphenols during DNA purification. Polyphenols are common in many plant tissues and can deactivate proteins if not removed and therefore inhibit many downstream reactions like PCR.

In microscopy, PVP is useful for making an aqueous mounting medium.[11]

Safety

The U.S. Food and Drug Administration (FDA) has approved this chemical for many uses,[12] and it is generally considered safe. However, there have been documented cases of allergic reactions to PVP/povidone, particularly regarding subcutaneous (applied under the skin) use and situations where the PVP has come in contact with autologous serum (internal blood fluids) and mucous membranes. For example, a boy having an anaphylactic response after application of PVP-Iodine for treatment of impetigo was found to be allergic to the PVP component of the solution.[13] A woman, who had previously experienced urticaria (hives) from various hair products, later found to contain PVP, had an anaphylactic response after povidone-iodine solution was applied internally. She was found to be allergic to PVP.[14] In another case, a man experiencing anaphylaxis after taking acetaminophen tablets orally was found to be allergic to PVP.[15]

Povidone is commonly used in conjunction with other chemicals. Some of these, such as iodine, are blamed for allergic responses, although testing results in some patients show no signs of allergy to the suspect chemical. Allergies attributed to these other chemicals may possibly be caused by the PVP instead.[16][17]

PVP has been widely used as surfactant, reducing agent, shape controlling agent and dispersant in nanoparticle synthesis and their self-assembly[18]

Hypoglycemic benefit of cinnamon, tea, witch hazel, cloves, bay leaf and allspice lost by treatment with polyvinylpyrrolidone. Broadhurst, JAFC 2000

Properties

PVP is soluble in water and other polar solvents. For example, it is soluble in various alcohols, such as methanol and ethanol,[19] as well as in more exotic solvents like the deep eutectic solvent formed by choline chloride and urea (Relin).[20] When dry it is a light flaky hygroscopic powder, readily absorbing up to 40% of its weight in atmospheric water. In solution, it has excellent wetting properties and readily forms films. This makes it good as a coating or an additive to coatings.

History

PVP was first synthesized by Walter Reppe and a patent was filed in 1939 for one of the most interesting derivatives of acetylene chemistry. PVP was initially used as a blood plasma substitute and later in a wide variety of applications in medicine, pharmacy, cosmetics and industrial production.[21][22]

Cross-linked derivatives

See also

References

  1. ↑ Haaf, F.; Sanner, A.; Straub, F. (1985). "Polymers of N-Vinylpyrrolidone: Synthesis, Characterization and Uses". Polymer Journal. 17: 143. doi:10.1295/polymj.17.143.
  2. ↑ Bühler, Volker (2005). Polyvinylpyrrolidone Excipients for Pharmaceuticals: Povidone, Crospovidone and Copovidone. Berlin, Heidelberg, New York: Springer. pp. 1–254. ISBN 3540234128. doi:10.1007/b138598.
  3. ↑ Ganesan, S; Felo, J; Saldana, M; Kalasinsky, V. F.; Lewin-Smith, M. R.; Tomashefski Jr, J. F. (2003). "Embolized crospovidone (polyN-vinyl-2-pyrrolidone) in the lungs of intravenous drug users". Modern Pathology. 16 (4): 286–92. PMID 12692192. doi:10.1097/01.MP.0000062653.65441.DA.
  4. ↑ PVP-Iodine. ispcorp.com. 2004.
  5. ↑ Das SK, Saha SK, Das A, Halder AK, Banerjee SN, Chakraborty M (2008). "A study of comparison of efficacy and safety of talc and povidone iodine for pleurodesis of malignant pleural effusions". Journal of the Indian Medical Association. 106 (9): 589–90, 592. PMID 19552086.
  6. ↑ Swei, J.; Talbot, J. B. (2006). "Development of high-definition aqueous polyvinylpyrrolidone photoresists for cathode ray tubes". Journal of Applied Polymer Science. 102 (2): 1637. doi:10.1002/app.23950.
  7. ↑ Chen, Tianming "Dental bleach", U.S. Patent 6,730,316, Priority date January 27, 2001
  8. ↑ Kavakka, J. S.; KilpeläInen, I.; Heikkinen, S. (2009). "General Chromatographic NMR Method in Liquid State for Synthetic Chemistry: Polyvinylpyrrolidone Assisted DOSY Experiments". Organic Letters. 11 (6): 1349–52. PMID 19231850. doi:10.1021/ol9001398.
  9. ↑ Fischer, Frank & Bauer, Stephan (2009). "Ein Polyvinylpyrrolidon (PVP): ein vielseitiges Spezialpolymer – Verwendung in der Keramik und als Metallabschreckmedium". Keramische Zeitschrift. 61 (6): 382–385.
  10. ↑ Göthlich, Alexander; Koltzenburg, Sebastian; Schornick, Gunnar (2005). "Funktionale Polymere im Alltag: Vielseitig". Chemie in Unserer Zeit. 39 (4): 262–273. doi:10.1002/ciuz.200400346.
  11. ↑ Lillie RD & Fullmer HM (1976) Histopathologic Technic and Practical Histochemistry, 4th ed. New York: McGraw-Hill, p. 411. ISBN 0-07-037862-2.
  12. ↑ Inactive Ingredients in FDA Approved Drugs. FDA/Center for Drug Evaluation and Research, Office of Generic Drugs, Division of Labeling and Program Support. Database Update Frequency: Quarterly. Data Through: January 6, 2010. Database Last Updated: January 13, 2010 – search on povidone for list of approved items
  13. ↑ Yoshida K, Sakurai Y, Kawahara S, et al. (2008). "Anaphylaxis to polyvinylpyrrolidone in povidone-iodine for impetigo contagiosum in a boy with atopic dermatitis". International Archives of Allergy and Immunology. 146 (2): 169–73. PMID 18204285. doi:10.1159/000113522.
  14. ↑ Adachi A, Fukunaga A, Hayashi K, Kunisada M, Horikawa T (March 2003). "Anaphylaxis to polyvinylpyrrolidone after vaginal application of povidone-iodine". Contact Dermatitis. 48 (3): 133–6. PMID 12755725. doi:10.1034/j.1600-0536.2003.00050.x.
  15. ↑ Rönnau AC, Wulferink M, Gleichmann E, et al. (November 2000). "Anaphylaxis to polyvinylpyrrolidone in an analgesic preparation". The British Journal of Dermatology. 143 (5): 1055–8. PMID 11069520. doi:10.1046/j.1365-2133.2000.03843.x.
  16. ↑ Katelaris, Constance (2009). "'Iodine Allergy' label is misleading". Australian Prescriber, Vol. 32, 125–128.
  17. ↑ van Ketel WG, van den Berg WH (January 1990). "Sensitization to povidone-iodine". Dermatologic Clinics. 8 (1): 107–9. PMID 2302848.
  18. ↑ Koczkur, Kallum M.; Mourdikoudis, Stefanos; Polavarapu, Lakshminarayana; Skrabalak, Sara E. "Polyvinylpyrrolidone (PVP) in nanoparticle synthesis". pubs.rsc.org. doi:10.1039/C5DT02964C. Retrieved 2015-12-15.
  19. ↑ Wohlfarth, C (2010). "Thermodynamic Properties of Polymer Solutions.". Landolt-Börnstein, New Series, Group VIII, Volume 6D. Springer Verlag. doi:10.1007/978-3-642-02890-8_752.
  20. ↑ Sapir, L.; Stanley, CB.; Harries, D. (2016). "Properties of Polyvinylpyrrolidone in a Deep Eutectic Solvent.". J. Phys. Chem. A. 120: 3253–3259. doi:10.1021/acs.jpca.5b11927.
  21. ↑ Fischer, Frank; Bauer, Stephan (2009). "Polyvinylpyrrolidon. Ein Tausendsassa in der Chemie". Chemie in unserer Zeit. 43 (6): 376–383. doi:10.1002/ciuz.200900492.
  22. ↑ Koczkur, Kallum M.; Mourdikoudis, Stefanos; Polavarapu, Lakshminarayana; Skrabalak, Sara E. "Polyvinylpyrrolidone (PVP) in nanoparticle synthesis". pubs.rsc.org. doi:10.1039/C5DT02964C. Retrieved 2015-12-15.
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