1.New drug R & D information need-based subject service
Chinese Journal of Medical Library and Information Science 2014;(5):47-49
After the information need characteristics of persons engaged in drug R & D were introduced, how to construct the embedded , follow-up and whole course subject service model was described , and suggestions were put forward for subject librarians to solve the problems at the time when the users meet through close cooperation with users by going out of library and placing themselves in the circumstances the users need.
2.Comparison of Transdermal Penetration of Two New Kinds of Triamcinolone Acetonide Lipid Carriers
Guoqiang WANG ; Zhaofeng LIANG ; Junfeng BAN ; Guanghan DENG ; Jiacheng LIN ; Zhufen LYU
Herald of Medicine 2015;(3):361-365
Objective To compare transdermal penetration of triamcinolone acetonide liposparticles (TAA-LPPs) and TAA-Ethosomes in vitro. Methods The TAA-LPPs and TAA-Ethosomes were produced and the morphology was observed by transmission electron microscope,particle size was detected by laser particle analyzer. The percutaneous permeability in vitro was tested by modified Franz diffusion pools. The amount of penetrated triamcinolone acetonide and the retention in the skin were de-termined by HPLC. Results The shape of TAA-LPPs and TAA-Ethosomes was almost spherical with mean diameter of (99. 9±1. 3) and (105±1. 4) nm, respectively. The cumulative transdermal penetration of TAA-LPPs, TAA-Ethosomess and TAA suspension was (53. 59±4. 40),(87. 03±4. 87),and (30. 54±8. 61) μg·(cm2 ) -1 , respectively . The drug retention in the skin after 32 h was (1. 02±0. 13), (0. 62±0. 08), (0. 55±0. 17) μg·(cm2 ) -1 , respectively. Conclusion TAA-LPPs is better for transdermal administration of triamcinolone acetonide by reducing systemic absorption of the drug.
3.Effects of Superfine Grinding Technology on Powder Properties and Dissolution of Oyster Shell
Zhenmiao QIN ; Jingying DENG ; Danlei ZHANG ; Junfeng BAN
China Pharmacy 2019;30(16):2216-2220
OBJECTIVE: To study the effects of superfine grinding on the powder properties and dissolution of oyster shell, and to provide experimental basis for its comprehensive exploitation. METHODS: Oyster shells were firstly prepared into ordinary powder by grinder. Then the ordinary powder was prepared into micro-powder Ⅰ (crushing 5 min) and Ⅱ (crushing 10 min) by ultrafine pulverizer. The differences of micromeritic properties were investigated before and after superfine grinding from the aspects of particle size distribution, specific surface area and porosity, angle of repose, bulk density, hygroscopicity, etc. Scanning electron microscope (SEM), Fourier transform infrared spectroscopy (FTIR) and X-ray powder diffraction (XRD) techniques were used to analyze the morphological characteristics and chemical structure of oyster shell before and after superfine grinding. The dissolution were investigated. RESULTS: Compared with ordinary powder, micropowder Ⅰ and micropowder Ⅱ’s were small in particle size and uniformly distributed, but the particles were easy to adhere and aggregate; the specific surface area, porosity and the angle of repose increased, while bulk density decreased; the hygroscopicity increased. FTIR and XRD showed no significant change in chemical structure of oyster shell after superfine grinding. The dissolution rate of micropowder Ⅱ and micropowder Ⅰ was 18.5% and 10.3% at 10 min, and the dissolution of ordinary powder was only 6.4% at 60 min. CONCLUSIONS: Compared with ordinary powder, oyster shell show obvious differences in powder properties after superfine grinding; the dissolution rate of the powders increases, and there is no significant change in chemical structure.
4.Preparation and Quality Evaluation of Imperatorin Ultradeformable Liposomes Gel
Xuehui CUI ; Shihong CHEN ; Jindi QIU ; Junfeng BAN ; Nannan YANG ; Qingchun NI ; Zhaoyan PAN ; Qingchun XIE ; Yanzhong CHEN ; Zhufen LYU
China Pharmacy 2020;31(9):1074-1079
OBJECTIVE:To prepare Imperatorin ultradeformable liposomes gel (IMP-UDLs-Gel),and to evaluate its quality. METHODS:Based on single factor test ,using 12 h accumulative penetration amount (Q12h)as evaluation index ,the proportion of carbomer 940,glycerol and propyl glycol in formulation of IMP-UDLs-Gel were investigated by orthogonal test. The optimal formulation was screened. The quality of IMP-UDLs-Gel prepared with the optimal formulation was evaluated. RESULTS :The optimal formulation of IMP-UDLs-Gel included carbomer 940 proportion of 1%,glycerol proportion of 15% and propyl glycol proportion of 10%. Q12 h of IMP-UDLs-Gel was (11.543±0.241)μg/cm2;the appearance was milky white and translucent ;the particle size was (93.13±1.68)nm,PDI was 0.268±0.012,Zeta potential was (-24.96±1.99)mV;pH was 7.32±0.03; viscosity was (45.37±1.27)g·s;steady flow was (0.727±0.002)μg·h/cm2,lag time was (4.358±0.175)h,apparent permeability coefficient was 1.392×10-3 cm/h,and it has good physical and optical stability. CONCLUSIONS :The preparation method is stable and feasible ,and the prepared IMP-UDLs-Gel has good adhesion ,stability and transdermal property.