• Title/Summary/Keyword: 경피흡수

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이온토포레시스에 의한 극성약물의 경피흡수 촉진

  • 심창구;김종국
    • Proceedings of the Korean Society of Applied Pharmacology
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    • 1992.05a
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    • pp.62-62
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    • 1992
  • 1.이온토포레시스에 의한 ISP의 경피촙수증가는 단순투과의 약 13배로서 그 증가정도는 전류세기와 약물농도에 비례하였다. 2. 가해주는 $Na^{+}$ 농도가 커질수록 ISP의 flux는 감소하였다. 3. ion-pairing agent률 가하면 ISP의 flux는 감소하는데, 그 감소정도는 TU>SAL>BEN 로서 이는 이 물질들이 ISP와 ion-pair를 형성하는 능력순서와 같았다. 4. ISP용액의 pH증가시 ISP의 flux는 대체적으로 증가하며 그 pattern은 피부의 pKa를 3.5로 가정할 때의 피부해리곡선과 유사하였다. ISP가 광범위한 pH에서 완벽하게 해리된다고 가정할 때 pH증가시 flux증가는 피부해리 증가에 따른 permselectivity 증가에 기인한 것으로 생각되었다.

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Preparation and Evaluation of Antibacterial Transdermal Device using Chitosan Matrices (키토산 매트릭스를 이용한 향균제 경피흡수제형의 제조와 평가)

  • Kim Sun Il;Na Jae Woon
    • Journal of the Korean Chemical Society
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    • v.37 no.5
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    • pp.527-536
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    • 1993
  • The characteristics of the controlled drug release were studied for biodegradable transdermal drug delivery system. A biodegradable polymeric matrix was prepared from chitosan, silver sulfadiazine, and glycerine. The release behavior of silver sulfadiazine from chitosan matrix was consistent with the Higuchi's diffusion controlled model. The release time was delayed by increasing the content of silver sulfadiazine and thickness of the matrix, whereas decreased as glycerine concentration increased. The apparent constant (K) of release rate was proportional to the content of drug or glycerine and the thickness of chitosan matrix. These results indicated that chitosan matrix shows some potential as a drug delivery system for transdermal therapeutic application.

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Enhancement of Skin Permeation of Wrinkle Improvement Peptides GHKs Using Liposomes Containing Skin Penetrating Peptides (피부 투과 펩티드가 함유된 리포좀을 이용한 주름 개선 펩티드 GHKs의 피부 흡수 증진)

  • Park, Su In;An, Gyu Min;Kim, Min Gi;Heo, Soo Hyeon;Shin, Moon Sam
    • Journal of the Korean Applied Science and Technology
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    • v.36 no.3
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    • pp.853-865
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    • 2019
  • In this study, the skin permeability was measured by adding skin penetrating peptides, arginine oligomers R4(tetra-D-arginine), R6(hexa-D-arginine) to little skin-permeable wrinkle improvement peptides GHK, GHK-Cu, and Pal-GHK liposomes, and the results were analyzed by the following six cases. (1) In cases where only wrinkle improvement peptides GHK, GHK-Cu, and Pal-GHK were contained liposomes; the final cumulative permeations in 24 hours were 6.05%, 7.4%, and 8.83% respectively. (2) In cases where arginine oligomers R4, R6 were added to GHK liposomes; the final cumulative permeations in 24 hours were 13.63% and 7.68%. (3) In cases where R4, R6 were added to GHK-Cu liposomes; the final cumulative permeations in 24 hours were 15.46% and 8.64%. (4) In cases where R4, R6 were added to Pal-GHK liposomes; the final cumulative permeations in 24 hours were 16.9% and 10.67%. (5) In cases where R4 were added to GHK, GHK-Cu, and Pal-GHK liposomes; the final cumulative permeations in 24 hours were 13.63%, 15.46%, and 16.9% respectively. (6) In cases where R6 were added to GHK, GHK-Cu, and Pal-GHK liposomes; the final cumulative permeations in 24 hours were 7.68%, 8.64%, and 10.67% respectively. This experiment showed that skin absorption of GHK was increased by copper ion (Cu2+) and palmitic acid and skin absorption of wrinkle improvement peptides was enhanced by cell penetrating peptides, and R4 showed higher effect than R6 in GHK, GHK-Cu and Pal-GHK. Through this process, we propose broad use and application in wrinkle improvement functional cosmetics by presenting the optimal conditions for increasing skin absorption of GHK, GHK-Cu, thus maximizing its efficacy.

이온토포레시스에 의한 피리도스티그민과 클로르페니라민의 in vitro 경피흡수

  • 심창구;김종국
    • Proceedings of the Korean Society of Applied Pharmacology
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    • 1993.04a
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    • pp.179-179
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    • 1993
  • 1. PS및 CP의 flux는 전류의 새기 및 donor의 약물농도에 비래하였다. 2. pH의 flux는 pH가 증가할수록 증가하였으나, CP(pKa=9.2)의 flux는 pH=2에서 최대치를 보였다. 이는 약물의 해리 정도와 H$^{+}$이온의 mobility, 또 피부의 permselectivity의 balance에 의해 결정된 것으로 생각된다. 3. donor cell에 NaCl을 첨가하면 두 약물 공히, 그러나 특히 PS의 flux가 저하되었다. 이는 두 약물의 이온과 $Na^{+}$의 mobility차이에 기인한다고 생각된다. 4. PS의 경우 taurodeoxycholate(TDC)같은 음이온을 donor cell에 공존시키면 flux가 감소하였다. 이는 PS와 TDC가 전기적으로 중성인 ion-pair complex를 형성함으로써 PS이온의 유효농도가 감소하기 때문으로 생각된다.

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Study on the preparation of Polymeric UV Screening agent using PVBC (PVBC계 고분자 자외선 차단제의 합성에 관한 연구)

  • 김효중;박혜상
    • Journal of the Society of Cosmetic Scientists of Korea
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    • v.22 no.1
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    • pp.70-83
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    • 1996
  • 자외선 차단제는 화장품 원료 중 주요 자극원의 하나이다. 그러나 자오선 차단제를 고분자로 만들 경우 피부에 도포 되었을 때 경피흡수가 불가능 하여 피부 자극 문제를 해결할 수 있다. 이에 본 연구에서는 PVBC와 alkylhydroxycinnamate를 반응시켜 고분자 자외선 차단제를 합성하였다, PVBC는 benzylic chloride를 가지고 있는 고분자로서 이 작용기는 친핵성 치환반응이 용이하므로 side chain modification이 가능하다. PVBC와 alkyl hydroxycinnamate의 반응에서 반응성은 alkyl hydroxycinnamate의 크기와 반응에 첨가된 촉매의 종류에 영향을 받는다. 효율이 낮은 촉매를 사용할 경우에는 alkyl hydroxycinnamate의 크기가 작을수록 반응수율이 높았으며, 높은 효율을 갖는 촉매를 사용할 경우에는 alkyl hydroxycinnamate의 종류에 관계없이 반응수율은 100%였다. 실험에 사용한 PVBC는 평균 분자량이 55,000이었으며, 고분자의 구조와 분자량은 NMR과 GPC로 확인하였다. 고분자 자외선 차단제의 자외선 흡수 능력은 OMC에 비해 65 - 94% 였으며, caprylic/capric triglyceride에 좋은 용해도를 보여주었다.

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Transdermal Permeation of Riboflavin in Ointment Bases Using Gums & Enhancers (Gum류의 연고제제와 흡수촉진제가 Riboflavin의 경피흡수에 미치는 영향)

  • 오세영;황성규;김판기
    • Journal of Environmental Health Sciences
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    • v.26 no.2
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    • pp.91-96
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    • 2000
  • We investigated characters of transdermal therapeutic system(TTS) and the skin permeability of that with applying drug delivery system(DDS). Natural gums were selected as material of TTS. The permeation of natural gums ointment containing drug in rat skin using diffusion cell model. Permeation properties of materials were investigated for water soluble drug such as riboflavin in vitro. We used glycerin, PEG 600 and oleic acid as enhancers. Since dermis has more hydration than the stratum corneum, skin permeation rate at steady state was highly influenced when glycerin was used in riboflavin. The permeation rate of content enhancer and drug was found to be faster than that of content riboflavin only. These results showed that skin permeation rate of drug across the composite was mainly dependent on the property of ointment base and drug. All the gum ointment tested showed good safety. Proper selection of the materials which resemble and enhance properties of the delivering drug was found to be important in controlling the skin permeation rate.

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Transdermal Delivery System of Effective Ingredients for Cosmeceuticals (기능성화장품을 위한 유효성분의 경피 전달 시스템)

  • Cho, Wan-Goo
    • Journal of the Society of Cosmetic Scientists of Korea
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    • v.37 no.2
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    • pp.97-119
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    • 2011
  • World consumers are now focusing on their health, well-being and appearance more than ever before. This trend is creating heightened demand for products formulated as cosmeceuticals with active ingredients. A significant number of innovative formulations are now being used in cosmetics with real consumer-perceivable benefits and optimized sensory attributes, resulting in an economic uplift of cosmetic industry. To obtain skin care formulations with real consumer-perceivable benefits through dermal delivery of active ingredients, formulators are resorting to technology that until recently was used in pharmaceutical products. These various delivery systems are now being used in cosmecuetical formulations. Novel delivery systems reviewed here possess enormous potential as next-generation smarter carrier systems.