Abstract:Investigating new possibilities for the application of 1% (v/v) iodophors, povidone-iodine (PVP-I) was better tolerated in the HET-CAM or explant test than 1% (w/v) silver nitrate or tetracycline. After application to the eye, at least 2.6% of used iodine were adsorbed. Therefore PVP-I is more effective than silver nitrate or erythromycin, meaning a possible alternative for the prevention of ophthalmia neonatorum. PVP-I is more active against methicillin-resistant Staphylococcus aureus (MRSA) in a human ex viv… Show more
“…This is in good agreement with the aforementioned in vitro observation that liposomal PVP-I is well tolerated in sensitive tissue [13,24] . The established allergic sensitization against seasonal grass pollen of some subjects played a major role in this study.…”
Section: Discussionsupporting
confidence: 92%
“…By treating infections or preventing their development PVP-I is providing secondary wound healing support [22,23] . Moreover, the liposomal formulation of PVP-I reduces cytotoxicity [24] and has been shown to promote wound healing in animal models [12] and in clinical studies [13] . Due to this established antiseptic property, PVP-I in conventional formulations has been used occasionally and successfully for nasal application, although neither the formulation nor the application mode were optimized for the nose [25,26] .…”
Section: Discussionmentioning
confidence: 99%
“…The data could be combined with the existing data of liposomal PVP-I on local tolerance and usefulness in moist wound healing combined with antisepsis [13] . The data suggest that the optimal PVP-I concentration is between 2.2 and 4.4%, since both concentrations scored best in different tests.…”
Section: Discussionmentioning
confidence: 99%
“…Liposomal PVP-I formulation possesses additional advantages with respect to tolerability and antiseptic efficacy, as shown in cell cultures, animal studies and (as a hydrogel) in wound healing studies in man [12,13] . Liposomes are vesicles of phospholipid bilayers and water.…”
Purpose of Study: This phase I study assessed tolerability and local effect of a liposome dispersion with povidone-iodine (polyvinylpyrrolidone-iodine, PVP-I) as nasal spray. Procedures: Three groups received liposomal dispersion with PVP-I (2.2, 4.4 and 0% as control) in single and repeated use (3 days, three times a day). A set of functional and cytological tests as well as safety assessments were performed. Results: No safety-relevant finding or serious adverse events were reported, no evidence for cyto- nor genotoxicity obtained. No clinically relevant changes in mucosa appearance, nor in olfactory sense, nor in ciliary activity (sensitive indicator of local tolerance) occurred and no complaints about nasal airflow obstruction were observed. All liposomal formulations had a positive effect on the nasal mucosa, challenged by allergy in some volunteers. Conclusions and Message: Application of liposomal PVP-I spray to the nasal mucosa does not result in any demonstrable limitation of the nasal function nor in detectable damage to the multilayer ciliated epithelium of the nose. Improvement of various parameters of nasal function under liposomal PVP-I suggest improved mucociliary clearance. Explanation could be humidification, improved surfactant (phospholipid) level and/or sufficient mucolytic activity of iodide due to local application of the constituents.
“…This is in good agreement with the aforementioned in vitro observation that liposomal PVP-I is well tolerated in sensitive tissue [13,24] . The established allergic sensitization against seasonal grass pollen of some subjects played a major role in this study.…”
Section: Discussionsupporting
confidence: 92%
“…By treating infections or preventing their development PVP-I is providing secondary wound healing support [22,23] . Moreover, the liposomal formulation of PVP-I reduces cytotoxicity [24] and has been shown to promote wound healing in animal models [12] and in clinical studies [13] . Due to this established antiseptic property, PVP-I in conventional formulations has been used occasionally and successfully for nasal application, although neither the formulation nor the application mode were optimized for the nose [25,26] .…”
Section: Discussionmentioning
confidence: 99%
“…The data could be combined with the existing data of liposomal PVP-I on local tolerance and usefulness in moist wound healing combined with antisepsis [13] . The data suggest that the optimal PVP-I concentration is between 2.2 and 4.4%, since both concentrations scored best in different tests.…”
Section: Discussionmentioning
confidence: 99%
“…Liposomal PVP-I formulation possesses additional advantages with respect to tolerability and antiseptic efficacy, as shown in cell cultures, animal studies and (as a hydrogel) in wound healing studies in man [12,13] . Liposomes are vesicles of phospholipid bilayers and water.…”
Purpose of Study: This phase I study assessed tolerability and local effect of a liposome dispersion with povidone-iodine (polyvinylpyrrolidone-iodine, PVP-I) as nasal spray. Procedures: Three groups received liposomal dispersion with PVP-I (2.2, 4.4 and 0% as control) in single and repeated use (3 days, three times a day). A set of functional and cytological tests as well as safety assessments were performed. Results: No safety-relevant finding or serious adverse events were reported, no evidence for cyto- nor genotoxicity obtained. No clinically relevant changes in mucosa appearance, nor in olfactory sense, nor in ciliary activity (sensitive indicator of local tolerance) occurred and no complaints about nasal airflow obstruction were observed. All liposomal formulations had a positive effect on the nasal mucosa, challenged by allergy in some volunteers. Conclusions and Message: Application of liposomal PVP-I spray to the nasal mucosa does not result in any demonstrable limitation of the nasal function nor in detectable damage to the multilayer ciliated epithelium of the nose. Improvement of various parameters of nasal function under liposomal PVP-I suggest improved mucociliary clearance. Explanation could be humidification, improved surfactant (phospholipid) level and/or sufficient mucolytic activity of iodide due to local application of the constituents.
“…In vitro, PVP-I diluted down to 0.125% is still microbicidally effective (>5 log CFU reduction) [13]. In rats, on the other hand, the healing of skin wounds is significantly delayed by 2% PVP-I [14], while 1.25% is tolerated in vitro by sensitive tissues such as nasociliary epithelium [15] and cartilage [16]. In the hen egg test on the chorioallantoic membrane, PVP-I 2.5% was shown to be irritative, but at a concentration of 1% was tolerated without reaction [17].…”
After preoperative conjunctival and periorbital antisepsis with povidone-iodine (PVP-I), the systemic absorption of iodine after cataract surgery was measured to evaluate the risk of thyroid side effects. Five different combinations of PVP-I alone or in combination with PVP-I-free antiseptics were applied to the conjunctiva and periorbital skin. An iodine-free product served as control. Iodide and creatinine in urine were analyzed before intervention and 24 and 48 h postoperatively. Depending on the concentration and application site, 0.3–4.5% of the total applied iodine or 3.6–45.4% of the free iodine were absorbed. The range of urine iodine excretion was between 11.7 and 71.0 µg iodine/g creatinine, depending on the PVP-I concentration and the site of application. The increase in iodine excretion was significant at 24 h postoperatively in trials receiving PVP-I both periorbitally and conjunctivally, depending of the concentration used. Because the iodine absorption is only slight and of doubtful clinical relevance, presurgical conjunctival antisepsis can be achieved with 1.25% PVP-I; so far clinically manifest anamnestic thyroid disorders are excluded. Presently, periorbital skin antisepsis with PVP-I cannot be recommended until data on thyroid metabolism in the population have been collected and evaluated, especially in a region currently or previously deficient in iodine.
This chapter introduces pyrrolidone chemistry as it relates to applications for skin. It begins with poly(vinyl pyrrolidone) (PVP) and its derivatives in skin care, and focuses on transdermal delivery of pharmaceutical ingredients and applications in wound care. Rheology modifiers are extremely important in personal care products and provide a product with a chassis that has a characteristic rheological profile. The chapter describes the application of small molecules (non‐polymeric) based on pyrrolidone chemistry in transdermal delivery and personal care. The transdermal patch is the most basic transdermal delivery system. The use of PVP in wound care mostly involves wound healing applications and antiseptics. PVP plays an extremely important role in nanotechnology. Both pyrrolidone carboxylic acid and sodium pyrrolidone carboxylate are used in many different types of skin care products, including lotions, creams, oils, cleansing formulas, sun care preparations, and makeup.
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