Transdermal anaesthesia with lidocaine nano-formulation pretreated with low-frequency ultrasound in rats model
Rapid local transdermal anaesthetic is desirable in clinic. In this paper, lidocaine loaded poly(epsilon-caprolactone)-poly(ethylene glycol)-poly(epsilon-caprolactone) (PCL-PEG-PCL) nanoparticles were prepared, and a novel transdermal lidocaine formulation: lidocaine loaded PCL-PEG-PCL nanoparticles in F127 hydrogel (Nano-Lido Gel), was demonstrated. These lidocaine loaded PCL-PEG-PCL nanoparticles with mean particle size of ca. 200 nm had drug loading of about 40%. The efficiency of transdermal anaesthesia of four treatments: EMLA cream (E), Nano-Lido Gel (N), EMLA cream with brief focal ultrasound pretreatment (EU), and Nano-Lidocaine Gel with brief focal ultrasound pretreatment (NU), was evaluated by tail-flick latency test assay in rats. Results indicated that the topical anaesthesia onset time in NU was 5 times and 2.5 times shorter than that in E and EU. The efficiency of anaesthesia in NU, expressed as maximum possible effects (MPE) value, was significantly higher than that in other treatments. It provided a novel path to develop rapid transdermal anaesthesia by combination of ultrasound pretreatment and lidocaine nano-formulation based on polymeric nanoparticles.
Medienart: |
Artikel |
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Erscheinungsjahr: |
2009 |
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Erschienen: |
2009 |
Enthalten in: |
Zur Gesamtaufnahme - volume:9 |
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Enthalten in: |
Journal of nanoscience and nanotechnology - 9(2009), 11 vom: 15. Nov., Seite 6360-5 |
Sprache: |
Englisch |
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Beteiligte Personen: |
Gou, MaLing [VerfasserIn] |
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Themen: |
98PI200987 |
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Anmerkungen: |
Date Completed 11.12.2009 Date Revised 15.07.2019 published: Print Citation Status MEDLINE |
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Förderinstitution / Projekttitel: |
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PPN (Katalog-ID): |
NLM192785621 |
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100 | 1 | |a Gou, MaLing |e verfasserin |4 aut | |
245 | 1 | 0 | |a Transdermal anaesthesia with lidocaine nano-formulation pretreated with low-frequency ultrasound in rats model |
264 | 1 | |c 2009 | |
336 | |a Text |b txt |2 rdacontent | ||
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338 | |a Band |b nc |2 rdacarrier | ||
500 | |a Date Completed 11.12.2009 | ||
500 | |a Date Revised 15.07.2019 | ||
500 | |a published: Print | ||
500 | |a Citation Status MEDLINE | ||
520 | |a Rapid local transdermal anaesthetic is desirable in clinic. In this paper, lidocaine loaded poly(epsilon-caprolactone)-poly(ethylene glycol)-poly(epsilon-caprolactone) (PCL-PEG-PCL) nanoparticles were prepared, and a novel transdermal lidocaine formulation: lidocaine loaded PCL-PEG-PCL nanoparticles in F127 hydrogel (Nano-Lido Gel), was demonstrated. These lidocaine loaded PCL-PEG-PCL nanoparticles with mean particle size of ca. 200 nm had drug loading of about 40%. The efficiency of transdermal anaesthesia of four treatments: EMLA cream (E), Nano-Lido Gel (N), EMLA cream with brief focal ultrasound pretreatment (EU), and Nano-Lidocaine Gel with brief focal ultrasound pretreatment (NU), was evaluated by tail-flick latency test assay in rats. Results indicated that the topical anaesthesia onset time in NU was 5 times and 2.5 times shorter than that in E and EU. The efficiency of anaesthesia in NU, expressed as maximum possible effects (MPE) value, was significantly higher than that in other treatments. It provided a novel path to develop rapid transdermal anaesthesia by combination of ultrasound pretreatment and lidocaine nano-formulation based on polymeric nanoparticles | ||
650 | 4 | |a Journal Article | |
650 | 4 | |a Research Support, Non-U.S. Gov't | |
650 | 7 | |a Anesthetics, Local |2 NLM | |
650 | 7 | |a Drug Carriers |2 NLM | |
650 | 7 | |a Lidocaine |2 NLM | |
650 | 7 | |a 98PI200987 |2 NLM | |
700 | 1 | |a Wu, Lan |e verfasserin |4 aut | |
700 | 1 | |a Yin, QinQin |e verfasserin |4 aut | |
700 | 1 | |a Guo, QingFa |e verfasserin |4 aut | |
700 | 1 | |a Guo, Gang |e verfasserin |4 aut | |
700 | 1 | |a Liu, Jin |e verfasserin |4 aut | |
700 | 1 | |a Zhao, Xia |e verfasserin |4 aut | |
700 | 1 | |a Wei, YuQuan |e verfasserin |4 aut | |
700 | 1 | |a Qian, Zhiyong |e verfasserin |4 aut | |
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