首页> 外文会议>Conference on laser-tissue interaction XI: Photochemical, photothermal, and photomechanical >Viability of Porcine Nasal Septal Cartilage Grafts Following Nd:YAG (lambda=1.32 mum) Laser Radiation
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Viability of Porcine Nasal Septal Cartilage Grafts Following Nd:YAG (lambda=1.32 mum) Laser Radiation

机译:猪鼻腔室隔膜包裹物的可行性以下Nd:YAG(Lambda = 1.32毫米)激光辐射

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Mechanically deformed morphologic cartilage grafts undergo a temperature dependent phase transformation during sustained laser irradiation that results in reshaping of the specimen. While thermal, optical, and mechanical properties of cartilage undergoing laser heating have been previously investigated, the viability of these irradiated grafts has yet to be examined closely until now. In this study, chondrocyte viability following laser irradiation was determined by measuring the incorporation of radiolabelled sulfate (Na ~(35)SO_4~(-2)) into proteoglycan (PTG) macromolecules. Proteoglycans are highly sulfated and are the principal molecular constituents of cartilage matrix. Their synthesis directly reflects chondrocyte viability. By measuring the scintillation counts of ~(35)SO_4~(-2) uptake and normalizing the value by the total protein content of each specimen we can determine the level of PTG synthesis rats following laser reshaping. Regional baseline PTG synthesis rates as a function of location was determined by dividing each specimen into six regions. All regions except the most cephalic are demonstrated similar PTG synthesis rates. The most cephalic region exhibited a significantly greater PTG synthesis rates. In order to establish a positive control for this study, specimens were immersed in boiling saline water for approximately 40 minutes. The boiled specimens demonstrated a fivefold increase in normalized radioisotope uptake and suggest that the non-specific uptake of radioactive Na~(35)SO_4~(-2) is caused by structural alterations in the collagen matrix caused by extensive thermal exposure. To avoid this thermal artifact, another positive control was established using nitric oxide was to induce apoptosis of the chondrocytes, resulting in significantly lower PTG synthesis compared to untreated tissue. Cartilage specimens (25 x 10 x 2 mm) were irradiated with light emitted from an Nd:YAG layser (25 W/cm2, lambda=1.32 mum) while specimens (25 x 10 x 2 mm) were irradiated with light emitted from an Nd:YAG laser (25 W/cm2, lambda=1.32 mum) while radiometric surface temperature, internal stress, and backscattered light were simultaneously recorded. Individual specimens underwent either one, two, or three sequential laser exposures with the duration of each exposure determined in real-time from observation of characteristic changes in integrated backscattered light intensity that correate with thermal mediated stress relaxation. A five-minute time interval between each irradiation was given to allow the cartilage to return to thermal equilibrium. Average laser exposure for each irradiation sequence was recorded (5, 8.3, 12.2 sec). PTG synthesis decreased with increasing laser exposure, but was noted to remain above baseline levels for NO treated tissue. To further refine these results and minimize the effect of regional tissue variations, 7 mm diameter discs excised from the most cephalic portions and a middle region of the pig nasal septal cartilages were irradiated. A reduction of PTG synthesis rates was noted with each successive irradiation, suggestign that laser mediated cartilage reshaping acutely does not eliminate the population of viable chondrocytes. The degree of reduction in PTG synthesis is dependent upon the time-temperature dependent heating profile created during laser irradiation, and carefully monitored dosimetry is necessary to ensure chondrocyte viability.
机译:机械变形形态学软骨移植物持续激光照射期间经受依赖于温度的相变的结果在试样的重塑。而经受软骨激光加热的热学,光学和机械性质先前已经研究了,这些照射移植物的生存力尚待仔细检查直到现在。在这项研究中,激光照射以下软骨细胞生存力通过测量放射性标记的硫酸盐(钠〜(35)SO_4〜(-2))掺入的蛋白聚糖(PTG)大分子确定。蛋白聚糖是高度硫酸化的和是软骨基质的主要分子成分。它们的合成直接反映软骨细胞活力。通过每个样品的总蛋白质含量测量〜(35)SO_4〜(-2)摄取的闪烁计数和归一化值,我们可确定PTG合成大鼠以下激光整形的水平。区域基线PTG合成速率作为位置的函数,通过将每个样品为六个区域来确定。除了最头侧所有地区都表现出类似的PTG合成速率。最头区域表现出显著更大PTG合成率。为了建立这项研究的阳性对照,试样浸在沸水盐水约40分钟。煮沸的样品展示了归一化的放射性同位素的摄取增加了五倍,并建议放射性娜〜(35)SO_4〜(-2)的非特异性摄取是通过在引起广泛的热暴露的胶原基质的结构改变而引起的。为了避免这种热伪影,另一种阳性对照,使用一氧化氮建立是诱导凋亡的软骨细胞,导致显著降低PTG合成相比,未经处理的组织。软骨试样(25×10×2mm)的用来自钕发射的光照射:YAG layser(25 W / cm 2时,波长= 1.32妈妈),而试样(25×10×2mm)的用来自钕发射的光照射:YAG激光(25 W / cm 2时,波长= 1.32妈妈),而辐射表面温度,内应力,和背向散射光同时记录。单个试样进行实时一个,两个,或与每个曝光的持续时间的三个连续激光照射从确定的特性的变化的观察中集成的反向散射光强度的是correate与热介导的应力松弛。被赋予各照射之间的五分钟的时间间隔,以允许软骨返回到热平衡。对于每个照射序列平均激光曝光记录(5,8.3,12.2秒)。 PTG合成随激光曝光减少,但有人指出,保持上述NO处理的组织的基线水平。为了进一步改善这些结果,并尽量减少区域组织变化的影响,直径7mm的光盘从最头侧部和鼻中隔软骨照射猪的中间区域切除。的PTG合成速率的降低与每一个连续的照射所指出的,suggestign激光介导的软骨重塑急性不会消除可行软骨细胞的群体。减少PTG合成的程度取决于激光照射期间产生的时间 - 温度依赖的加热分布,并仔细监测剂量测定是必要的,以确保软骨细胞生存力。

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