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5%聚维酮碘乳膏对铜绿假单胞菌烧伤创面感染的杀菌效果

Bactericidal efficacy of 5 per cent povidone iodine cream in Pseudomonas aeruginosa burn wound infection.

作者信息

De Wet P M, Rode H, Cywes S

机构信息

Department of Paediatric Surgery, University of Cape Town, Red Cross Children's Hospital, Rondebosch, South Africa.

出版信息

Burns. 1990 Aug;16(4):302-6. doi: 10.1016/0305-4179(90)90145-m.

Abstract

A new topical antiseptic agent, 5 per cent polyvinylpyrrolidone-iodine (PVP-I) cream, with altered physicochemical properties, incorporated in a different carrier base has proved in vivo to be more effective in controlling burn wound infections than 10 per cent PVP-I ointment. Important biodynamic properties of the new formulation have not, however, been elucidated in vivo. Hence the need for a controlled study to evaluate the bioavailability of the active component after penetration through burn eschar; the bactericidal efficacy of the cream and determination of the bactericidal time of the cream in comparison with 10 per cent PVP-I ointment. A modified Walker burn wound model was used to define the rate of trans-eschar penetration, biodynamic availability and bactericidal efficacy of 5 per cent povidone iodine cream in established Pseudomonas aeruginosa burn wound infection. In vitro penetration confirmed the effective diffusion of PVP-I cream through 1.5 mm eschar within 6 h. A single topical application of PVP-I cream resulted in a 98.8 per cent (6.088 x 10(9) c.f.u./g of tissue to 7.367 x 10(7) c.f.u./g of tissue) reduction in intra-eschar viable organisms within 18 h after application. A second topical application of PVP-I cream at 18 h resulted in a total reduction of 99.8 per cent in viable organisms (2.90 x 10(9) c.f.u./g of tissue to 7.009 x 10(6) c.f.u./g of tissue) within 48 h. Comparing the in vitro bactericidal time of povidone iodine ointment with cream against Pseudomonas aeruginosa, Staphylococcus aureus and a Klebsiella pneumoniae revealed that the PVP-I cream killed organisms ten-fold more quickly than the ointment.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

一种新型局部抗菌剂,即5%聚乙烯吡咯烷酮碘(PVP-I)乳膏,其理化性质有所改变,并采用了不同的载体基质。经体内实验证明,与10% PVP-I软膏相比,它在控制烧伤创面感染方面更有效。然而,这种新制剂的重要生物动力学特性尚未在体内得到阐明。因此,需要进行一项对照研究,以评估活性成分透过烧伤焦痂后的生物利用度;该乳膏的杀菌效果,并与10% PVP-I软膏比较确定该乳膏的杀菌时间。采用改良的沃克烧伤创面模型来确定5%聚维酮碘乳膏在已形成的铜绿假单胞菌烧伤创面感染中的透焦痂渗透速率、生物动力学可用性和杀菌效果。体外渗透实验证实PVP-I乳膏在6小时内可有效透过1.5毫米的焦痂。单次局部应用PVP-I乳膏后,应用后18小时内焦痂内活菌数量减少了98.8%(从6.088×10⁹ 菌落形成单位/克组织降至7.367×10⁷ 菌落形成单位/克组织)。在18小时时第二次局部应用PVP-I乳膏,48小时内活菌总数减少了99.8%(从2.90×10⁹ 菌落形成单位/克组织降至7.009×10⁶ 菌落形成单位/克组织)。比较聚维酮碘软膏和乳膏对铜绿假单胞菌、金黄色葡萄球菌和肺炎克雷伯菌的体外杀菌时间发现,PVP-I乳膏杀灭细菌的速度比软膏快十倍。(摘要截选至250字)

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