• 한국정밀공학회:학술대회논문집
• /
• 한국정밀공학회 2010년도 춘계학술대회 논문집
• /
• pp.1433-1434
• /
• 2010

• 한국응용약물학회:학술대회논문집
• /
• 한국응용약물학회 1996년도 춘계학술대회
• /
• pp.286-286
• /
• 1996

In order to elucidate the mechanism of action of transdermal absorption-enhancing compounds, i.e., pyrrolidone derivatives (2-pyrrolidone, 1-methyl-2-pyrrolidone, 1-ethyl-2-pyrrolidone, 1,5-dimethyl-pyrrolidone and 5-methyl-2-pyrrolidone), multilamellar liposome was prepared from the simulated stratum corneum lipid and employed as a model system for the barrier function of the stratum corneum. The liposomal membrane of the stratum corneum lipid liposome (SCLL) behaves as an osmometer and has an excellent barrier function. In addition, its phase transition temperatures are similar to those of human stratum corneum intercellular lipid region. Therefore, SCLL seems to be a useful skin model. To estimate the barrier function of SCLL, the osmotic behavior of SCLL was measured in the presence of pyrrolidone derivatives and the effect on the phase transition temperature of SCLL was also investigated using differential calorimetry. Above a certain concentration (MLAC), enhances perturb the barrier function of the liposome. The relationship between MLACs and the partition coefficient of the pyrrolidone derivatives was observed; the greater the partition coefficients, the smaller the MLAC. This suggests that the more hydrophobic enhancers penetrate into the lipid layer more easily and reduce the barrier function of membrane more effectively. The results of differential scanning thermograms of the SCLL suggest that the pyrrolidone derivatives had incorporated into the lipid layer in the liposome and increased the fluidity of the lipid layer in the liposome. Such activity might have some correlation with the transdermal absorption-enhancing activity these compounds.

• International Journal of Precision Engineering and Manufacturing
• /
• 제9권3호
• /
• pp.68-71
• /
• 2008

Transdermal and topical drug delivery with minimal tissue damage has been an area of vigorous research for a number of years. Our research team has initiated the development of an effective method for delivering drug particles across the skin (transdermal) for systemic circulation, and to localized (topical) areas. The device consists of a micro particle acceleration system based on laser ablation that can be integrated with endoscopic surgical techniques. A layer of micro particles is deposited on the surface of a thin metal foil. The rear side of the foil is irradiated with a laser beam, which generates a shockwave that travels through the foil. When the shockwave reaches the end of the foil, it is reflected as an expansion wave and causes instantaneous deformation of the foil in the opposite direction. Due to this sudden deformation, the microparticles are ejected from the foil at very high speeds, and therefore have sufficient momentum to penetrate soft body tissues. We have demonstrated this by successfully delivering cobalt particles $3\;{\mu}m$ in diameter into gelatin models that represent soft tissue with remarkable penetration depth.

• 대한화장품학회지
• /
• 제37권2호
• /
• pp.97-119
• /
• 2011

전 세계의 소비자들은 예전에 비해 외모, 건강 및 안락한 삶에 관심을 집중시키고 있다. 이와 같은 경향은 유효성분을 함유한 기능성화장품의 요구 또한 증대시키고 있다. 차별화된 제형을 이용한 감각적인 사용감이 구현된 처방은 실질적인 소비자 인지 수준의 화장품에 이용되고 있으며 그 결과로 화장품시장이 확대되고 있다. 이와 더불어 유효성분의 경피 전달을 통한 소비자 인지 수준의 제품을 개발하기 위해서 화장품 과학자는 첨단 의약품의 다양한 기술을 접목해야 한다. 다양한 경피 흡수 수단의 기술이 기능성 화장품에 사용되고 있다. 본 총설에서는 차세대 경피 전달 시스템으로서 큰 잠재력을 가진 경피 전달 시스템에 대해서 논하고자 한다.

• KSBB Journal
• /
• 제16권3호
• /
• pp.253-258
• /
• 2001

항고지단백혈증제제를 이용한 경펴투과제제흘 제조하고자 기 재로서 xathan gum을 사용하여 약물의 함량 및 투과 촉전제에 따라서 경피투과체제를 제조하고 경피투과 항고지단백혈증제의 가능성 등을 연구하였다. 기재로 사용한 xanthan gum의 체 타전위를륜 측정하여 응결, 침전이 나타나는 등천점으로부터 제타전위 값의 차이가 나타나 있으므로 피부와 접촉시 연고제제외 석출 가능성이 없다는 것을 확인할 수 있었다. 각각의 지용성과 수용성 항고지단백혈증제제를 함유한 정피투과제제를 사용하여 진행된 투과 실험에서는 자용성인 clofibrat$\xi$의 투파속도가 현저하게 빠르게 나타났는데 이는 지용성인 피부 각질과의 친화 즉 lipophilicity를 증가시킴으로써 지용성인 clofibrate의 경피투과를 촉진시키는 것이라 생각된다. 지용성 경피투과제제에 투과촉진제를 첨가했을 경우, 그렇지 않은 경우에 비해 lag time파 투과속도가 빠르게 나타냈다. 특히 PEG 600을 사용했윤 경우가 가장 빠른 투과속도흘 나타냈고 글리세린, 올레산의 순오로 투과속도의 증가를 나타냈다. PEG 600븐 다른 투과촉진제보다 지용성 약물인 clofibrate에 대해 피부내의 지방과 단백겔의 유동성(fluidity) 과 피부 각질의 lipophilicity를 증가시컴으로서 각질로의 약물분배를 촉진한다고 생각된다.

• 대한약학회:학술대회논문집
• /
• 대한약학회 2002년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.2
• /
• pp.409.2-409.2
• /
• 2002

Retinol is widely used for skin care. the improvement of the appearance of aging. photo-damaged or oxidatively stressed skin. and especially for the improvement of the appearance of wrinkled skin. Retinol. however. is extremely sensitive to atmospheric oxygen. and easily decomposed by exposure to air. Retinol is commonly formulated as the ointments or creams for cosmetic preparations. (omitted)

• Journal of Pharmaceutical Investigation
• /
• 제33권1호
• /
• pp.21-28
• /
• 2003

Ketorolac tromethamine(KT) is a nonsteroidal agent with potent analgesic and moderate anti-inflammatory activity. The lipid-water partition coefficient of KT was evaluated and KT gel was formulated as a gel containing different pH, different concentrations of polymer (poloxamer 407, carbopol 941), propylene glycol, ethanol and various enhancers. The resulting KT gels were evaluated with respect to their viscosity, in vitro drug permeation rate through hairless mouse skin and stability. In n-octanol and chloroform, the lipid-water partition coefficient of KT was the highest at pH 4 phosphate buffer. The apparent viscosity of KT gel increased with an increase in gel pH, polymer and enhancer concentration. But the apparent viscosity of KT gel decreased with an increase in ethanol concentration. The permeation rate of KT through hairless mouse skin from gels different pH was maximum at pH 4 which is close to KT $pK_{a}$ 3.54. The permeation rate decreased with an increase in polymer, propylene glycol concentration. But the permeation rate increased with an increase in ethanol. The increase of drug concentration from 1 to 3% induced linear increase in permeation rate. The best enhancer was the combination of $Labrasol^{\circledR},\;Transcutol^{\circledR}$, oleic acid and l-menthol. In the accelerated stability test(25, 40 and $50{\circ}C$), pH 5 gel was most stable and pH 4 gel was most unstable for 90 days.

• The Journal of Korean Physical Therapy
• /
• 제14권4호
• /
• pp.147-162
• /
• 2002

Transdermal permeation enhancer has been used to increased skin absorption. External control of drug release and skin absorption can also be achieved by iontophoresis or phonophoresis. However, because several problems with iontophoresis are that it has a risk to skin damage because of the change of pH and the increase of current density in applying it and that it can be applied only in the form of water solution, This study is to enhance drug permeation via skin following application of ultrasound. For this goal, in gel containing piroxicam, the degree of skin permeation in vitro and anti-inflammatory effect in in vivo were investigated. Permeation study using hairless mouse skin was performed at 37 $^{\circ}C$ using buffer saline as the receptor solution. The amount of piroxicam were quantified using a HPLC system consisting of solvent delivery system. Following adoption of ultrasound 1 MHZ, it showed relatively high permeation rate where it was compared with non treated by ultrasound. The influence of duty cycle having an effect on skin permeation rate was slight higher in the case of using pulsed mode. Skin permeation increase attended by intensity of ultrasound, the permeation of trice was accelerated at 2.0 W/$cm^{2}$ than 1.0 W/$cm^{2}$. The skin permeation of piroxicam was substantially influenced by ultrasound. Anti-inflammatory effects were determined using carrageenan-induced paw swelling method in SD rat. Paw swelling tests showed that pulsed phonophoresis group was more effective than control group and only gel application group. The conclusion of phonophoresis was found to improve significantly the skin permeation in vitro and the anti-inflammatory effect in vivo.

• Journal of Pharmaceutical Investigation
• /
• 제29권4호
• /
• pp.329-335
• /
• 1999

Clenbuterol, a selective ${\beta}_2-adrenergic$ receptor stimulant, has been introduced as a potent bronchodilator for patients with bronchial asthma, chronic bronchitis and pulmonary emphysema. For the purpose of developing a transdermal preparation for clenbuterol, we attempted to select an optimal solvent system and permeation enhancer among fatty acids and fatty alcohols which are known to accelerate the penetration of various drugs in permeation experiments using hairless mouse skin and Franz diffusion cell. Apparent partition coefficient of clenbuterol was increased as pH of buffer solution was increased and solubility of clenbuterol was increased as the percent of propylene glycol(PG) in buffer solution(pH 10) was increased. Permeability of clenbuterol from different buffer(pH 10)/PG solvent mixtures was decreased as the percent of PG in pH 10 buffer solution was increased and among the various enhancers studied, lauryl alcohol was found to be the most effective enhancer, increasing the permeability of clenbuterol approximately 76-fold compared with control. Lauryl alcohol$(0{\sim}2%)$ enhanced the permeability of clenbuterol concentration-dependently. In this study, the optimal solvent system for the penetration of clenbuterol was found to be 50/50 buffer(pH 10)/PG solvent mixture containing 2% lauryl alcohol.

• 융합정보논문지
• /
• 제11권8호
• /
• pp.212-223
• /
• 2021

본 연구는 스피큘이 함유된 화장품을 피부에 적용하였을 때 안전한지를 평가하고, 기능성 활성 물질이 담지된 다이아몬드-스피큘이 경피흡수를 높이면서 피부에는 효율적으로 투과되어 그 효능이 잘 나타나는지 검토하는 데 목적을 두었다. 이를 위하여 30~60대 여성 30명을 대상으로 각 시험군에 따른 화장품을 4주간 피부에 적용하여 주관적으로 느끼는 피부 자극 및 피부 변화 여부를 설문지를 통하여 조사하였다. 그 결과 스피큘을 함유한 화장품이 일반 화장품과 비교하여 피부에 더 안전하였으며, 특히 다이아몬드-스피큘 함유화장품의 경우는 항주름, 탄력, 보습, 미백, 염증 완화 및 예민함 등이 시험 전과 비교하여 월등하게 개선되었다고 통계적으로도 유의미한 응답을 하였다(p<.001). 이로써 스피큘이 함유된 화장품이 피부에 안전하며, 기능성 활성 물질이 담지된 다이아몬드-스피큘이 경피전달시스템의 기능뿐 아니라 담지된 활성 물질이 피부에 효율적으로 투과될 수 있는 다기능성 화장품 소재로의 활용도 가능함을 확인하였다.