Palma S D, Maletto B, Lo Nostro P, Manzo R H, Pistoresi-Palencia M C, Allemandi D A
Departamento de Farmacia, Facultad de Ciencias Químicas, Universidad Nacional de Córdoba, Argentina.
Drug Dev Ind Pharm. 2006 Aug;32(7):821-7. doi: 10.1080/03639040500534150.
6-O-Ascorbic acid alkanoates (ASCn) are amphiphilic molecules having physical-chemical properties that depend on the alkyl chain length. The derivatives of low molecular weight (n < 11) have enough aqueous solubility to produce self-assemblies at room temperature ( approximately 25 degrees C), while those with longer alkyl chains possess a critical micellar temperature (CMT) higher than 30 degrees C. At higher temperatures (T degrees > CMT), ASCn aqueous suspensions turn into either micellar solutions or gel phases, depending on the length of the hydrophobic chain. On cooling, coagels are produced, which possess a lamellar structure that exhibit sharp X-ray diffraction patterns and optical birefringence. The semisolid consistency of such coagels is an interesting property to formulate dermatological pharmaceutical dosage forms able to solubilize and stabilize different drugs. The objective of the present study was the evaluation of the enhancing permeation effect of ASCn with different chain lengths and to correlate permeability changes with histological effects. With this purpose, ASCn coagels containing anthralin (antipsoriasic drug) or fluorescein isothiocyanate (FITC, hydrophobic fluorescent marker) were assayed on rat skin (ex vivo) and mice skin (in vivo), respectively. Also, histological studies were performed aimed at detecting some possible side effects of ASCn. No inflammatory cellular response was observed in the skin when ASCn coagels were applied, suggesting non-irritating properties. Light microscopy indicated slight disruption and fragmentation of stratum corneum. The penetration of ASCn through rat skin epidermis was very fast and quantitatively significant. The permeation of anthralin was significantly increased when the drug was vehiculized in ASCn coagels, compared to other pharmaceutical systems. The results indicated that ASC12 seems to have the highest enhancing effect on FITC permeation. ASC12 appears to be the compound that possesses the highest capacity to enhance the penetration of the drugs. Furthermore, it has the highest permeation of the serie.
6 - O - 抗坏血酸链烷酸酯(ASCn)是具有取决于烷基链长度的物理化学性质的两亲性分子。低分子量(n < 11)的衍生物具有足够的水溶性,能够在室温(约25℃)下产生自组装,而具有较长烷基链的衍生物的临界胶束温度(CMT)高于30℃。在较高温度(T℃ > CMT)下,ASCn水悬浮液根据疏水链的长度转变为胶束溶液或凝胶相。冷却时,会产生具有层状结构的共凝胶,该结构呈现出尖锐的X射线衍射图案和光学双折射。这种共凝胶的半固体稠度是配制能够溶解和稳定不同药物的皮肤病学药物剂型的一个有趣特性。本研究的目的是评估不同链长的ASCn的促渗透作用,并将渗透率变化与组织学效应相关联。为此,分别在大鼠皮肤(体外)和小鼠皮肤(体内)上测定了含有蒽林(抗银屑病药物)或异硫氰酸荧光素(FITC,疏水性荧光标记物)的ASCn共凝胶。此外,进行了组织学研究,旨在检测ASCn的一些可能的副作用。当应用ASCn共凝胶时,在皮肤中未观察到炎症细胞反应,表明其具有非刺激性。光学显微镜显示角质层有轻微破坏和碎片化。ASCn穿过大鼠皮肤表皮的渗透非常快且在数量上很显著。与其他药物系统相比,当药物以ASCn共凝胶为载体时,蒽林的渗透率显著增加。结果表明,ASC12似乎对FITC渗透具有最高的增强作用。ASC12似乎是具有最高增强药物渗透能力的化合物。此外,它在该系列中具有最高的渗透率。