Coad C T, Osato M S, Wilhelmus K R
Am J Ophthalmol. 1984 Nov;98(5):548-51. doi: 10.1016/0002-9394(84)90238-1.
We undertook an in vitro investigation of the role of the design of the eyedrop dispenser in bacterial contamination. The nozzle tips of pipette and squeeze bottles containing Fluress (pH 5.0) were inoculated with 10 microliter of an ocular isolate of Pseudomonas aeruginosa (5.5 X 10(5) bacteria/ml). Cultures of single drops of ophthalmic solution (25-microliter drops from each pipette bottle and 40-microliter drops from each squeeze bottle) were done one minute, 15 minutes, one hour, two hours, and 24 hours after inoculation. Swabs from the inside of the caps of the eyedrop bottles were also cultured at similar intervals. No bacteria were recovered from either dispenser type after one hour. Swabbings from the caps of the pipette bottles showed no growth within minutes after inoculation, but swabbings from the caps of the squeeze bottles consistently yielded bacteria for 24 hours. We suggest that the cap of the squeeze bottle serves as a potential reservoir for bacterial contamination whereas direct contact of microorganisms with the preservative in an ophthalmic solution by the use of a pipette-type dispenser decreases the risk of microbial contamination and growth.
我们对滴眼剂分配器的设计在细菌污染中所起的作用进行了一项体外研究。将含有氟米龙(pH 5.0)的移液管和挤压瓶的喷嘴尖端接种10微升铜绿假单胞菌眼部分离株(5.5×10⁵ 细菌/毫升)。在接种后1分钟、15分钟、1小时、2小时和24小时,对眼科溶液的单滴培养物(每个移液瓶滴出25微升,每个挤压瓶滴出40微升)进行培养。滴眼剂瓶瓶盖内部的拭子也在相似的时间间隔进行培养。1小时后,两种类型的分配器均未培养出细菌。移液瓶瓶盖的拭子在接种后几分钟内没有生长,但挤压瓶瓶盖的拭子在24小时内持续培养出细菌。我们认为,挤压瓶的瓶盖可作为细菌污染的潜在储存器,而使用移液管型分配器使微生物与眼科溶液中的防腐剂直接接触,可降低微生物污染和生长的风险。