Conventional techniques developed for the production of liposomes for ocular delivery show low encapsulation efficiencies (EE). In this work, a supercritical CO2 based one-step continuous process, named Supercritical Assisted Liposome formation (SuperLip), was used for the production of liposomes to deliver ophthalmic antibiotics, such as ampicillin and ofloxacin. Micrometric and sub-micrometric liposomes with mean diameters in the range from 280 ± 104 nm to 1.76 ± 0.79 μm were successfully produced using drug concentrations in the range from 1% to 6% w/w and water to lipid ratios from 1.7 mg/g to 25 mg/g. Encapsulation efficiencies up to 97% and 99% were obtained for ofloxacin and ampicillin respectively. Storage stability and drug release kinetics of produced liposomes were also studied. Liposomes were stable for at least 3 months, with negligible drug leakage during storage time. At 37 °C ofloxacin and ampicillin were released in a controlled manner within 3 and 4 h respectively.
Supercritical assisted process for the efficient production of liposomes containing antibiotics for ocular delivery / Campardelli, R.; Trucillo, P.; Reverchon, E.. - In: JOURNAL OF CO2 UTILIZATION. - ISSN 2212-9820. - 25:(2018), pp. 235-241. [10.1016/j.jcou.2018.04.006]
Supercritical assisted process for the efficient production of liposomes containing antibiotics for ocular delivery
Trucillo P.Secondo
;
2018
Abstract
Conventional techniques developed for the production of liposomes for ocular delivery show low encapsulation efficiencies (EE). In this work, a supercritical CO2 based one-step continuous process, named Supercritical Assisted Liposome formation (SuperLip), was used for the production of liposomes to deliver ophthalmic antibiotics, such as ampicillin and ofloxacin. Micrometric and sub-micrometric liposomes with mean diameters in the range from 280 ± 104 nm to 1.76 ± 0.79 μm were successfully produced using drug concentrations in the range from 1% to 6% w/w and water to lipid ratios from 1.7 mg/g to 25 mg/g. Encapsulation efficiencies up to 97% and 99% were obtained for ofloxacin and ampicillin respectively. Storage stability and drug release kinetics of produced liposomes were also studied. Liposomes were stable for at least 3 months, with negligible drug leakage during storage time. At 37 °C ofloxacin and ampicillin were released in a controlled manner within 3 and 4 h respectively.File | Dimensione | Formato | |
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