• 제목/요약/키워드: Tissue penetration

검색결과 142건 처리시간 0.028초

초단파 레이저 조사시 티슈 열완화 시간 분석 (Analysis of Thermal Relaxation Time of Tissues Subject to Pulsed Laser Irradiation)

  • 김경한;이제훈;서정
    • 한국레이저가공학회지
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    • 제12권2호
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    • pp.17-25
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    • 2009
  • Two methodologies for predicting thermal relaxation time of tissue subjected to pulsed laser irradiation is introduced by the calculation the optical penetration depth and by the investigation of the temperature diffusion behavior. First approach is that both x-axial and y-axial thermal relaxation times are predicted and they are superposed to achieve the thermal relaxation time (${\tau}_1$) for two-dimensional square tissue model. Another approach to achieve thermal relaxation time (${\tau}_2$) is measuring the time required for local temperature drop until $e^{-1}$ of the maximum laser induced heating.

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컴퓨터 알고리즘에 의한 표면온도와 레이저 열전도에 관한 연구 (Study on the Surface Temperature and Laser Heat Conduction by the Computer Algorithm)

  • 이영욱
    • 정보학연구
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    • 제9권3호
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    • pp.67-75
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    • 2006
  • This study deals with the computing the temperature change of surface to the increment of time and diffusivity, the heat flux during irradiation of laser. In addition, the computer algorithm for computing the penetration change of the corresponding surface irradiated is developed. The result of this study shows the possibility to treatment of cancer, abnormal cell and biological tissue during irradiation of laser.

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치아경조직의 약물 침투에 관한 연구 (Study for Medicinal Penetration in Dental Tissue)

  • 양동규
    • 대한치과의사협회지
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    • 제11권4호
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    • pp.271-276
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    • 1973
  • This study is concerned with the effect on Penetration of varing the length of time among the applications of stains, preparations of medicine and radio-active isotope of siver in 120 carious or non carious human teeth with a vital pulp. The study revealed the following conclusions : 1) The stains and preparations penetrated through the dentinal tube and it's seem to be ceased at zone of secondary dentinal area. 2) The stains and preparations did not penetrated in enamel tissues.

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인체 대장암세포 다층배양계에서 파크리탁셀의 투과 (Penetration of Paclitaxel in Multicellular Layers of Human Colorectal Cancer Cells)

  • 최미선;박종국;알-압드 아메드;구효정
    • Journal of Pharmaceutical Investigation
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    • 제36권6호
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    • pp.385-392
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    • 2006
  • Paclitaxel is an important chemotherapeutic agent for the treatment of human solid tumors. Multicellular resistance(MCR) is considered to be a major mechanism of resistance of human solid tumors to chemotherapeutic agent such as paclitaxel, which includes barriers to drug penetration through tumor tissues. Multicellular layers(MCL) cultures resemble in vivo tumor condition in terms of MCR and has been used successfully to produce clinically relevant data. In the present study, we evaluated the penetration characteristics and post-penetration anti-proliferative activity of paclitaxel using MCL of human colorectal cancer cells(DLD-1 and HT-29) grown in Transwell inserts. The penetration of $[^{14}C]-paclitaxel$ was slower than that of mannitol which penetrates via paracellular pathway in DLD-1 MCL. The penetration of $[^{14}C]-paclitaxel$ was faster in HT-29 MCL compared to DLD-1 MCL, i.e., at 10 ${\mu}M$ 100% and 40% penetration were observed after 48 hr incubation for HT-29 and DLD-1 cells, respectively. When calculated using anti-proliferative activity in the conditioned media of bottom chamber, the penetration after 24 hr was very limited(less than 50%) and concentration-dependent at the concentrations tested in both MCL's. These results suggest that limited and differential penetration of paclitaxel in tumor tissues may contribute to lower and differential efficacy against human solid tumors.

조직공학을 위한 생체모사용 스캐폴드 개발 (Development of Biomimetic Scaffold for Tissue Engineering)

  • 박수아;이준희;김완두
    • Elastomers and Composites
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    • 제44권2호
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    • pp.106-111
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    • 2009
  • 조직공학은 기능을 상실한 인체를 대체하거나 복원하기 위해 인공대체품을 개발하기 위한 중요한 학문이다. 특히, 세포가 자랄 수 있는 지지체 역할을 하는 스캐폴드는 조직공학 연구를 위한 중요한 부분을 차지하고 있다. 그래서, 3차원 조직공학용 스캐폴드 개발을 위한 다양한 제조 방법을 소개하고자 하였다. 스캐폴드의 일반적인 제조방법으로는 염침출법 (solvent-casting particulate-leaching), 염 발포법 (gas foaming/salt leaching), fiber meshes/fiber bonding 법, 상분리법 (phase separation), melt moulding 법, 동결 건조법 (freeze drying)이 있으며, 넓은 표면적을 가진 스캐폴드 개발방법으로 전기방사법이 알려져 있다. 또한, 최근에는 스캐폴드 내부의 균일한 세포의 침투를 유도하기 위해 적당한 공극크기를 조절하고 우수한 공극률을 가진 스캐폴드를 개발하고자 stereolithography (SLA), selective laser sintering (SLS), fused deposition modeling (FDM), 및 3D printing (3DP) 와 같은 다양한 solid freeform fabrication (SFF) 기술이 개발되어지고 있다.

Prediction of Pharmacokinetics and Penetration of Moxifloxacin in Human with Intra-Abdominal Infection Based on Extrapolated PBPK Model

  • Zhu, LiQin;Yang, JianWei;Zhang, Yuan;Wang, YongMing;Zhang, JianLei;Zhao, YuanYuan;Dong, WeiLin
    • The Korean Journal of Physiology and Pharmacology
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    • 제19권2호
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    • pp.99-104
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    • 2015
  • The aim of this study is to develop a physiologically based pharmacokinetic (PBPK) model in intra-abdominal infected rats, and extrapolate it to human to predict moxifloxacin pharmacokinetics profiles in various tissues in intra-abdominal infected human. 12 male rats with intra- abdominal infections, induced by Escherichia coli, received a single dose of 40 mg/kg body weight of moxifloxacin. Blood plasma was collected at 5, 10, 20, 30, 60, 120, 240, 480, 1440 min after drug injection. A PBPK model was developed in rats and extrapolated to human using GastroPlus software. The predictions were assessed by comparing predictions and observations. In the plasma concentration versus time profile of moxifloxcinin rats, $C_{max}$ was $11.151{\mu}g/mL$ at 5 min after the intravenous injection and $t_{1/2}$ was 2.936 h. Plasma concentration and kinetics in human were predicted and compared with observed datas. Moxifloxacin penetrated and accumulated with high concentrations in redmarrow, lung, skin, heart, liver, kidney, spleen, muscle tissues in human with intra-abdominal infection. The predicted tissue to plasma concentration ratios in abdominal viscera were between 1.1 and 2.2. When rat plasma concentrations were known, extrapolation of a PBPK model was a method to predict drug pharmacokinetics and penetration in human. Moxifloxacin has a good penetration into liver, kidney, spleen, as well as other tissues in intra-abdominal infected human. Close monitoring are necessary when using moxifloxacin due to its high concentration distribution. This pathological model extrapolation may provide reference to the PK/PD study of antibacterial agents.

구강내 면역계에 대한 기본 고찰

  • 김성민
    • 대한치과의사협회지
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    • 제40권8호통권399호
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    • pp.620-627
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    • 2002
  • Oral health depends on the intergrity of the oral mucosa for prevention of the penetration of microbes and macromolecules that might be infectious, allergenic or antigenic. The intraoral immune systems include the tonsils, adenoids and nasopharyngeal-associated lymphoreticular tissue, or NALT. Mucosal inductive sites of the gastrointestinal tract(Peyer's patches and the appendix) and solitary lymph nodes collectively compose the gut-associated lymphoreticualr tissue, or GALT system. Both NALT and GALT are inductive regions where foreign antigens derived from viruses, bacteria, yeast and other molecules are encountered. The integration of tissues in NALT and GALT as part of the mucosal immune system, is very important to keep the oral immune system.

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치과용(齒科用) Cement하(下)에서의 Liner의 작용(作用)에 관(關)한 실험적(實驗的) 연구(硏究) (An Experimental Study on the Role of Liners under Dental Cements)

  • 양원식;김영수
    • 대한치과보철학회지
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    • 제8권1호
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    • pp.90-94
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    • 1968
  • The author attempted to study the role of liners as a barrier against the penetration of the acids released from the liquid of dental cements. Six different kinds of liners were used in this study and the depth of penetration of the acids of phosphate and silicate cements were measured ands following conclusions were obtained. 1. All the liners successfully prevented penetration of the acids released from phosphate and silicate cements. 2. When silicate cements were placed into the cavity without any liners, free acids were liberated continuously and thus may give injuries to the pulp tissue.

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Study on biopolymer delivery system and effect of wound healing with polysaccharide extracted from Agaricus blazei Murill

  • Kim, Min-Kyoung;Lee, Hye-Young;Hong, Eock-Kee
    • 한국생물공학회:학술대회논문집
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    • 한국생물공학회 2005년도 생물공학의 동향(XVII)
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    • pp.816-820
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    • 2005
  • Polysaccharide-based dressings have increasingly become viable alternatives to somewhat less biocompatible and often problematic cotton or viscose gauzes traditionally used for wound dressings. Polysaccharide which is particularly abundunt in Agaricus blazei Murill is known as the bioactive materials. Polysaccharide extracted from Agaricus blazei Murill enhances the recovery of the damaged epidermal tissue and the production of epithelial cell growth factors which are necessary to heal the burn and wound on the epidermal tissue. In this study, the biopolymer delivery system of polysaccharide extracted from Agaricus blazei Murill into epidermal tissue was elucidated using the skin permeating enhancer in vitro. The enhancing effects of various penetration enhancers and some other enhancers on the permeation of ${\beta}-glucan$ were evaluated using Franz diffusion cell. Permeation of polysaccharide in nomal and burn skin was compared. Polysaccharide was studied for the burn and wound healing activity in the epidermal tissue on rats.

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Photoresponsive Hydrogels as Drug Delivery Systems

  • Abueva, Celine DG.;Chung, Phil-Sang;Ryu, Hyun-Seok;Park, So-Young;Woo, Seung Hoon
    • Medical Lasers
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    • 제9권1호
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    • pp.6-11
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    • 2020
  • Hydrogels have been developed and used in tissue engineering and regenerative medicine to deliver therapeutics to injured or diseased tissue because of their versatility and properties that can be tailored to match the natural extracellular matrix. Hydrogels can be made with a variety of physical and chemical properties combined with light responsiveness ideal for applications in different fields of medicine that require the spatiotemporal control of therapeutics. Light, as a stimulus, is relatively inexpensive, contact-free, noninvasive with high spatial resolution and temporal control, convenient and easy to use, and allows deep tissue penetration that is relatively harmless. Photoresponsive hydrogels are ideal candidates for on-demand drug delivery systems that are capable of sustained and controlled drug release, minimizing the side effects, and ensuring the activity and efficient delivery of drugs to the target tissue.