• 대한한방소아과학회지
• /
• 제20권2호
• /
• pp.177-196
• /
• 2006

Objective : This experimental study was designed to determine the effects of BPT on obesity in vivo and in vitro. Methods : in vitro, BPTn extracts of various concentration(50, 100, 200 ${\mu}g/m{\ell}$) were added in 3T3-L1 cell. Adipocyte differentiation was measured by Oil Red O staining and Morphological examination. The expression of $C/EBP{\alpha}$ and $PPAR{\gamma}$ receptor was measured by western blot assay and RT-PCR in vivo, Rats were orally administered BPT daily for consecutive four weeks before poloxamer-407 induced hyperlipidemic state. The rats were sacrificed 24 hrs later for poloxamer-407 treated and then serum triglyceride, total cholesterol were measured ; Rats were orally administered BPT daily for consecutive four weeks before triton WR-1339 induced hyperlipidemic state. The rats were sacrificed 40 hrs later for triton WR-1339 treated and then serum triglyceride, total cholesterol were measured ; Rats with obesity were induced by the high fat-diet for six weeks and then serum triglyceride, total cholesterol, LDL-cholesterol, triglyceride, HDL-cholesterol, hydroxy radical, superoxide dismuatse activity were measured. Results : In vitro, The 3T3-L1 cells' differentiation was significantly decreased by BPT. The expression of $C/EBP{\alpha}$ and $C/EBP{\beta}$ was decreased by BPT. In vivo, BPT significantly reduced serum triglyceride, total cholesterol contents in poloxamer-407 treated rat. BPT significantly reduced serum triglyceride contents in Triton WR-1339 treated rat. Total cholesterol also reduced but did not show a significant change. BPT significantly reduced body weight gain of rat and adipose tissue mass of rats and serum triglyceride, LDL-cholesterol contents and significantly increased HDL-cholesterol, HTR(HDL-cholesterol/Total-cholesterol) in rats with obesity induced by the high fat-diet. BPT reduced blood lipid peroxide, hydroxy radical and increased superoxide dismuatse(SOD) activity.

• 대한비뇨기종양학회지
• /
• 제15권3호
• /
• pp.178-186
• /
• 2017

Purpose: Poloxamer 407 (P407) thermo-sensitive hydrogel formulations were developed to enhance the retention time in the urinary bladder after intravesical instillation. Materials and Methods: P407 hydrogels (P407Gels) containing 0.2 w/w% fluorescein isothiocyanate dextran (FD, MW 4 kDa) as a fluorescent probe were prepared by the cold method with different concentrations of the polymer (20, 25, and 30 w/w%). The gel-forming capacities were characterized in terms of gelation temperature (G-Temp), gelation time (G-Time), and gel duration (G-Dur). Homogenous dispersion of the probe throughout the hydrogel was observed by using fluorescence microscopy. The in vitro bladder simulation model was established to evaluate the retention and drug release properties. P407Gels in the solution state were administered to nude mice via urinary instillation, and the in vivo retention behavior of P407Gels was visualized by using an in vivo imaging system (IVIS). Results: P407Gels showed a thermo-reversible phase transition at $4^{\circ}C$ (refrigerated; sol) and $37^{\circ}C$ (body temperature; gel). The G-Temp, G-Time, and G-Dur of FD-free P407Gels were approximately $10^{\circ}C-20^{\circ}C$, 12-30 seconds, and 12-35 hours, respectively, and were not altered by the addition of FD. Fluorescence imaging showed that FD was spread homogenously in the gelled P407 solution. In a bladder simulation model, even after repeated periodic filling-emptying cycles, the hydrogel formulation displayed excellent retention with continuous release of the probe over 8 hours. The FD release from P407Gels and the erosion of the gel, both of which followed zero-order kinetics, had a linear relationship ($r^2=0.988$). IVIS demonstrated that the intravesical retention time of P407Gels was over 4 hours, which was longer than that of the FD solution (<1 hour), even though periodic urination occurred in the mice. Conclusions: FD release from P407Gels was erosion-controlled. P407Gels represent a promising system to enhance intravesical retention with extended drug delivery.

• 대한화장품학회지
• /
• 제49권1호
• /
• pp.17-27
• /
• 2023

본 연구에서는 탈모방지 토너의 활성 성분인 tocopheryl acetate, salicylic acid 및 niacinamide 성분 중 유용성 성분인 tocopheryl acetate의 피부흡수를 높이기 위한 연구를 진행하였다. Salicylic acid와 niacinamide를 함유함과 동시에 tocopheryl acetate를 투명하게 가용화시키려는 방법으로, 계면활성제가 회합하여 형성되는 micelle의 크기를 증가시킨 swollen micelle 구조를 이용하였다. 제조한 swollen micelle 용액은 3종의 활성 성분을 함유하며 투명한 성상과 안정성을 높이기 위해 계면활성제로 poloxamer 407과 octyldodeceth-16을 사용하였다. 또한 micelle의 크기를 증가시키기 위한 보조계면활성제로서 isostearic acid를 사용하였다. 제조한 swollen micelle의 물리적 특성을 평가하기 위해 실온(25 ℃)에서의 탁도를 측정하였다. Swollen micelle에 함유된 탈모방지 성분 중, tocopheryl acetate의 피부흡수율을 평가하기 위해 Franz diffusion cell method를 이용하였다. 24 h 후 tocopheryl acetate의 경우 대조군보다 6 배 향상된 피부흡수량을 보여주었다. 따라서 본 연구에서 개발한 swollen micelle은 탈모방지 제품 또는 여러 기능성 화장품의 가용화 제형에 응용될 수 있음을 알 수 있다.

• International Journal of Industrial Entomology and Biomaterials
• /
• 제3권1호
• /
• pp.1-6
• /
• 2001

Silk protein has been investigated by many researchers to apply to biomedical field. We reviewed biomedical applications of silk protein such as matrix of wound dressing and drug delivery system. Since silk fibroin/ poly (ethylene glycol) (PEG) semi-interpenetrating polymer networks showed good mechanical properties and wound healing phenomena, it can be used as wound dressing materials. Sericin nanoparticles pre- pared by conjugation with PEG and silk protein/ poloxamer mixture gel are expected to become a deliv- ery as matrix for hydrophobic drug.

• 한국응용약물학회:학술대회논문집
• /
• 한국응용약물학회 1996년도 춘계학술대회
• /
• pp.274-274
• /
• 1996

1차적인 제형의 조제를 위해서 비이온성 계면활성제인 poloxamer 류, Tween 류, octylphenylether와 양심 계면활성제인betaine 류와 방부제인 croquat 류에 대한 시험을 실시하여 자극을 나타내지 않은 성분을 선별하였다. 이를 근거로 isotonic sodium borate 용액을 완충액으로 사용하여, 최종제형을 조제하여 시험한 결과 자극반응을 나타내지 알았으며, 본 제형을 실온과 4$0^{\circ}C$에서 2, 4, 6개월간 안정성 시험을 거친 후 시험시에도 전혀 자극반응을 나타내지 않았다.

• 대한약학회:학술대회논문집
• /
• 대한약학회 2003년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.1
• /
• pp.121-121
• /
• 2003

The purpose of this study is to investigate the effect of mucosal vaccine delivery vehicles and adjuvants on the local and systemic antibody responses following mucosal immunization of mice with hepatitis B surface antigen (HBsAg). Mice were immunized on days 0 and 21 by administration of hepatitis B surface antigen B (HBsAg) into the vagina. HBsAg was delivered in saline or poloxamer(Pol)-based vehicle containing mucoadhesive polycarbophil (PC). (omitted)

• Bulletin of the Korean Chemical Society
• /
• 제30권2호
• /
• pp.486-488
• /
• 2009

• 한국잠사학회:학술대회논문집
• /
• 한국잠사학회 2005년도 제48회 추계 학술연구 발표회
• /
• pp.29-29
• /
• 2005

• Bulletin of the Korean Chemical Society
• /
• 제30권1호
• /
• pp.1-3
• /
• 2009

• 대한약학회:학술대회논문집
• /
• 대한약학회 2002년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.2
• /
• pp.411.2-411.2
• /
• 2002

In order to develope an optimum formulation for iontophoretic delivery of vitamine-C-2 phosphate. we have prepared 3 different formulations using hydrophilic polymers, such as poloxamer, carbo pol and HPMC and iontophoretic flux through skin from these hydrogel formulations was carried out. The effect of current density, drug concentration and current profile on flux was investigated. In-vitro flux study was performed at 36.5$^{\circ}C$, using side-by-side diffusion cell. Full-thickness hairless mouse skin was used for this work. (omitted)