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| 1 | Incorporation methods for cholic acid chitosan-g-mPEG self-assembly micellar system containing camptothecin显示文摘 | Tanasait Ngawhirunpat Nanthida Wonglertnirant Praneet Opanasopit Uracha Ruktanonchai Rangrong Yoksan Kaewkarn Wasanasuk Suwabun Chirachanchai | 2009 | Colloids and Surfaces B: Biointerfaces2009，，1： | 1 |
| 2 | Transdermal delivery of fluorescein isothiocyanate-dextrans using the combination of microneedles and low-frequency sonophoresis显示文摘This study aimed to evaluate the patient-friendly methods that are used in the delivery of hydrophilic macromolecules into deep skin layers,in particular,the combination of microneedles patch(MNs patch)and low-frequency sonophoresis(SN).The hydrophilic macromolecule drug fluorescein isothiocyanate(FITC)-dextrans(FD-4:MW 4.4 kDa)was used as the model drug in our experimental design.In this study,excised porcine skin was used to investigate and optimize the key parameters that determine effective MNs-and SNfacilitated FD-4 delivery.In vitro skin permeation experiments revealed that the combination of MNs patch with SN had a superior enhancing effect of skin permeation for FD-4 compared to MNs alone,SN alone or untreated skin,respectively.The optimal parameters for the combination of MNs and SN included the following:10 N insertion force of MNs,4 W/cm^(2)SN intensity,6 mm radiation diameter of the SN probe,2 min application time,and the continuous mode duty cycle of SN.In addition,vertical sections of skin,clearly observed under a confocal microscope,confirmed that the combination of MNs and SN enhanced permeation of FD-4 into the deep skin layers.These studies suggest that the combination of MNs and SN techniques could have great potential in the delivery of hydrophilic macromolecules into deep skin. | Boonnada Pamornpathomkul Sureewan Duangjit Suvida Laohapatarapant Theerasak Rojanarata Praneet Opanasopit Tanasait Ngawhirunpat | 2015 | Asian Journal of Pharmaceutical Sciences2015，10，5： | 1 |
| 3 | Incorporation of camptothecin into N-phthaloyl chitosan-g-mPEG self-assembly micellar system显示文摘 | PRANEET O TANASAIT N AMORNRUT C | 2006 | Eur J Pharm Biopharm2006，64，3： | 1 |
| 4 | Development and characterization of pectinate micro/ nanoparticles for gene delivery显示文摘 | Praneet Opanasopit Auayporn Apirakaramwong Tanasait Ngawhirun- pat | 2008 | AAPS Pharm Sci Tech2008，9，1： | 1 |
| 5 | Incorporation ofcamptothecin into N-phthaloyl chitosan-g-Mpeg self-assemblymicellar system显示文摘 | Praneet O Tanasait N Amornrut C | 2006 | European Journal of Pharmaceutics andBiopharmaceutics2006，64，26： | 1 |
| 6 | Lysozyme-loaded, electrospun chitosan-based nanofiber mats for wound healing显示文摘 | Natthan Charernsriwilaiwat Praneet Opanasopit Theerasak Rojanarata Tanasait Ngawhirunpat | 2012 | International Journal of Pharmaceutics2012，，2： | 1 |
| 7 | One-enzymecatalyzed simultaneous plant cell disruption and conversion ofreleased glycoside to aglycone combined with in situ productseparation as green one-pot production of genipin from gardenia fruit显示文摘 | Weerapath W Praneet O Tanasait N Theerasak R | 2013 | Enzyme and Microbial Technology2013，53，： | 1 |
| 8 | De-velopment and characterization of pectinate micro/nanop-articles for gene delivery显示文摘 | PRANEET O AUAYPORN A TANASAIT N | 2008 | Aaps Pharmscitech2008，9，1： | 1 |
| 9 | Design and development of optimal invasomes for transdermal drug delivery using computer program显示文摘Capsaicin(CAP)is a major pungent component that has been widely studied in medical and pharmaceutical fields.CAP was used both orally and topically for pain relief.However,the extreme pungency and the water insolubility of CAP lead to its restriction in the development of CAP as drug delivery system[1].Our previous study suggested that the computer software exhibited a beneficial role in the development of menthosomes for transdermal drug delivery[2].To confirm the reliability and reproducibility of simultaneous optimal formulations,the optimal ultraflexible liposomes(invasomes)estimated by the computer software(Design Expert?)were experimentally formulated and investigated. | Sureewan Duangjit Tassanan Nimcharoenwan Nutcha Chomya Natthporn Locharoenrat Tanasait Ngawhirunpat | 2016 | Asian Journal of Pharmaceutical Sciences2016，11，1： | 0 |
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