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Bio-Synthesis of Silver Nanoparticle Using Azadirachta indica Leaves 印楝叶生物合成纳米银颗粒的研究
Pub Date : 2019-06-14 DOI: 10.4172/2324-8777.1000263
N. Geetha, D. Prakash, Kumar Vs
In this study, simple approach was attempted to obtain a green eco-friendly way for the bio-synthesis of metal nanoparticles (AgNPs) from bioreduction of AgNO3 solutions using Azadirachta indica leaf extracts. The formation of nanoparticle and its stability were examined through UV-Visible spectra, FTIR spectra, and Zeta potential measurements. The exposure of metal ions to these plant extract by UV-Vis confirmed the presence of silver nanoparticles. FTIR revealed the reduction of silver ions, the functional groups present in the plant extract. The stability of the AgNPs was confirmed with the zeta potential measurement.
本研究以印楝叶提取物为原料,通过生物还原AgNO3溶液,试图获得一种绿色环保的生物合成金属纳米颗粒(AgNPs)的方法。通过紫外可见光谱、FTIR光谱和Zeta电位测试,考察了纳米颗粒的形成及其稳定性。金属离子暴露于这些植物提取物的紫外线-可见证实了银纳米粒子的存在。FTIR显示了植物提取物中官能团银离子的还原。zeta电位测定证实了AgNPs的稳定性。
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引用次数: 0
Morphological Characterization of Nanointerconnects Formed at the Interface of Sn Coated Multiwalled Carbon Nanotubes on an Etching Mask Patterned on a Si Substrate 硅衬底蚀刻掩模上锡包覆多壁碳纳米管界面纳米互连的形态表征
Pub Date : 2019-06-14 DOI: 10.4172/2324-8777.1000265
M. Us, Li-Jie Ci, Lin Kl
Tin-coated multiwalled carbon nanotube (SnO2/MWCNT) composites were synthesized by precipitation of SnCl2 within a CNT suspension in the first stage. An efficient dispersion technique using trifluroacetic acid (TFA) has been employed for the homogenous dispersion of Sn coated multiwalled carbon nanotubes (MWCNT) on an etching mask patterned on Si wafer using AZ 1500 as a photoresist. The MWCNT suspension was dispersed homogenously on the patterned Si wafer and the formation of nano-interconnects or nanojoints were clearly established by high-resolution transmission electron spectroscopy (HRTEM). High Resolution Transmission Electron Microscopy (HRTEM) images demonstrated that nano-interconnects formed between two MWCNTs consisted of both tetragonal Sn and orthorhombic SnO2 phase. .Elemental Sn was observed at the interface of two multiwalled carbon nanotubes by reduction of SnO2/MWCNTs under a reflow atmosphere. The interfacial interaction between the graphene layers in the carbon nanotubes and metallic Sn/oxides were also investigated. Raman spectroscopy studies established the interfacial interaction between MWCNT and the metallic Sn. The results revealed that the strong interaction between MWCNT and Sn lowered the ID/IG ratio in MWCNTs. The multiwalled carbon nanotubes were found to be well connected to each other on the patterned mask and this phenomenon could throw new light on the conductivity of carbon nanotubes in electronic circuits.
第一阶段在碳纳米管悬浮液中沉淀SnCl2,合成了锡包覆多壁碳纳米管(SnO2/MWCNT)复合材料。采用三氟乙酸(TFA)在硅片蚀刻掩模上均匀分散锡包覆的多壁碳纳米管(MWCNT)。通过高分辨率透射电子能谱(HRTEM), MWCNT悬浮液均匀地分散在图像化硅片上,并清晰地建立了纳米互连或纳米接头的形成。高分辨率透射电镜(HRTEM)图像表明,两种MWCNTs之间形成的纳米互连既包括四方相Sn,也包括正交相SnO2。在回流气氛下,通过还原SnO2/MWCNTs,在两种多壁碳纳米管的界面上观察到单质Sn。研究了碳纳米管中石墨烯层与金属锡/氧化物的界面相互作用。拉曼光谱研究建立了MWCNT与金属锡之间的界面相互作用。结果表明,MWCNTs与Sn之间的强相互作用降低了MWCNTs中的ID/IG比。发现多壁碳纳米管在图案掩膜上相互连接良好,这一现象可以为电子电路中碳纳米管的导电性提供新的思路。
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引用次数: 0
Facile Synthesis of 1D and 2D Zinc Sulfide Nanostructures on Multi-Layered Graphene 多层石墨烯上一维和二维硫化锌纳米结构的简易合成
Pub Date : 2019-06-14 DOI: 10.4172/2324-8777.1000266
Allon Sm, H. Al-Shukaili, T. Mohiuddin, S. Karthikeyan, R. Al-Busaidi
ZnS nanostructures have been fabricated over multi-layered graphene substrate via chemical vapor deposition technique. A controllable morphology of grown ZnS nanostructures, including (1D) nanowires, (2D) discs and nano-flakes were achieved by direct carbo-thermal evaporation of (1:1) ZnS and graphite powders mixture. The substrate location and therefore its temperature was found as a crucial growth parameter, which controls the morphology of the grown ZnS Nanostructures. The average diameter of the ZnS 1-D nanowires, at T= 400 °C, 2-D planar filling nano-discs, at T=300 °C, are 0.418 ± 0.007 μm, 0.600 ± 0. 020 μm respectively. At lower substrate temperature, <300 °C, a periodic round shaped features or flakes with some nanowire at their edges were formed due to nanodiscs amalgamation. This is because at a lower temperature, higher liquid instability leads to more nucleation sites and high conversion rate from liquid to solid state and therefore small nano-discs will merge to form larger flake structure. All products are cubic sphalerite ZnS in structure and with preferentially intense (111) planes. The lattice parameter for (220) planes was 5.72 A with 5.92% strain % clearly indicate that they are in tensile stress region. Raman was utilized to define the existence of graphene layers and the ZnS nanostructures (Magnified range100-700 cm-1) on top of multigraphene layers before and after growth process. In addition, ZnS nanostructures PL emissions of violet and cyan-blue centered at 3.23ev and (2.41-2.53ev) respectively were detected and attributed to defects such as Zn2+ vacancies, S2− interstitials, and dislocations. Graphene-based inorganic hybrid nanostructures deliver several potential applications in optoelectronics and nanoscale electronics such as photodetectors, photovoltaic and optical devices.
利用化学气相沉积技术在多层石墨烯衬底上制备了ZnS纳米结构。通过直接碳热蒸发(1:1)的ZnS和石墨粉混合物,获得了可控制的生长ZnS纳米结构,包括(1D)纳米线、(2D)纳米片和纳米片。发现衬底位置及其温度是一个关键的生长参数,它控制着生长的ZnS纳米结构的形貌。在温度为400℃时,zns1 -d纳米线的平均直径为0.418±0.007 μm,在温度为300℃时,二维平面填充纳米片的平均直径为0.600±0 μm。020 μm。在较低的衬底温度(<300°C)下,由于纳米片的合并,形成了周期性的圆形特征或边缘有纳米线的薄片。这是因为在较低的温度下,较高的液体不稳定性导致更多的成核位点和高的液体到固体的转化率,因此小的纳米圆盘会合并形成较大的片状结构。所有产品在结构上均为立方闪锌矿ZnS,具有优先强的(111)平面。(220)平面的点阵参数为5.72 A,应变%为5.92%,处于拉应力区。利用拉曼光谱来确定生长前后石墨烯层和ZnS纳米结构(放大范围100-700 cm-1)在多层石墨烯层上的存在。此外,还检测到了以3.23ev和(2.41 ~ 2.53ev)为中心的紫色和蓝蓝色ZnS纳米结构的PL发射,并将其归因于Zn2+空位、S2−间隙和位错等缺陷。基于石墨烯的无机杂化纳米结构在光电子学和纳米电子学领域有许多潜在的应用,如光电探测器、光伏和光学器件。
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引用次数: 0
Understanding the UV-Vis Spectroscopy for Nanoparticles 了解纳米颗粒的紫外可见光谱
Pub Date : 2019-06-14 DOI: 10.4172/2324-8777.1000268
Q. Abbas
UV-Vis technique is a compulsory technique for the optical study of the materials. Optical study helps the researcher for the application s of nanomaterials for different uses. Different devices are fabricat- ed on the basis of optical properties of the materials especially solar cells. With the help of this technique optical band gap can be calcu- lated which helps to choose the materials for the energy conversion purpose like light energy to electrical energy in solar cell. Also, from this technique purity of the sample can be measured by comparison with the reference solution. Here results of different materials are described which can help to better understand the analysis of Uv- Vis spectroscopy results.
紫外可见技术是材料光学研究的必修技术。光学研究有助于研究人员将纳米材料应用于不同的用途。根据材料特别是太阳能电池的光学特性,可以制作出不同的器件。利用该技术可以计算光带隙,从而为太阳能电池中光能转换为电能的材料的选择提供依据。同时,通过与参比溶液的比较,可以测定样品的纯度。本文介绍了不同材料的分析结果,有助于更好地理解紫外可见光谱分析结果。
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引用次数: 12
Optimization of Ohmic Contact Fabrication for Al0.3Ga0.7N/AlN/GaN HEMTs on 6H-SiC Using Recess Etching and Surface Plasma Treatment Processes 基于凹槽刻蚀和表面等离子体处理工艺的6H-SiC上Al0.3Ga0.7N/AlN/GaN hemt欧姆接触工艺优化
Pub Date : 2019-06-14 DOI: 10.4172/2324-8777.1000267
Gunjan Rastogi, R. Kaneriya, Santanu Sinha, R. Upadhyay
Ohmic contacts to AlGaN/AlN/GaN heterostructures with low contact resistance and smooth surface morphology play a vital role in the development of high power, high frequency GaN transistors. In the present work, two different Ohmic contact fabrication techniques, recess etching and surface plasma treatment, are optimized in order to obtain good Ohmic contact performance on undoped AlGaN/AlN/ GaN heterostructure on 6H-SiC substrate.For Ohmic contact fabrication, Ti/Al/Ni/Au metallization scheme is studied under optimized Rapid Thermal Annealing (RTA) temperature and time. Three samples are prepared with different recess based process flow and surface plasma treatment. Standard Transmission Line Model (TLM) is used for computation of contact resistance, sheet resistance and specific contact resistance of Ohmic contacts. For the first time, we explored feasibility of surface plasma treatment process for fabricating Ohmic contacts on AlGaN/ AlN/GaN based heterostructures. We achieved contact resistance of around 0.27 Ω*mm. Further to it we realized improvement in contact resistance on AlGaN/AlN/GaN based heterostructures using recess etching and achieved contact resistance of around 0.25 Ω*mm using Ti/Al/Ni/Au metal stack. Based on the characterization results it is also observed that surface plasma treatment process is a good alternative of comparatively complex recess etching process in fabricating Ohmic contacts for AlGaN/AlN/GaN based High Electron Mobility Transistors (HEMTs).
具有低接触电阻和光滑表面形貌的AlGaN/AlN/GaN异质结构欧姆接触对大功率、高频GaN晶体管的发展起着至关重要的作用。为了在6H-SiC衬底上获得良好的未掺杂AlGaN/AlN/ GaN异质结构欧姆接触性能,本文对凹槽刻蚀和表面等离子体处理两种不同的欧姆接触制备工艺进行了优化。对于欧姆接触制备,在优化的快速热退火(RTA)温度和时间下,研究了Ti/Al/Ni/Au金属化方案。采用不同的工艺流程和表面等离子体处理方法制备了三种样品。采用标准传输线模型(TLM)计算欧姆触点的接触电阻、片电阻和比接触电阻。我们首次探索了表面等离子体处理工艺在AlGaN/ AlN/GaN异质结构上制造欧姆触点的可行性。我们实现了约0.27 Ω*mm的接触电阻。此外,我们通过凹槽刻蚀实现了AlGaN/AlN/GaN基异质结构接触电阻的改善,并通过Ti/Al/Ni/Au金属堆叠实现了约0.25 Ω*mm的接触电阻。基于表征结果还发现,表面等离子体处理工艺是制备高电子迁移率晶体管欧姆触点的一个很好的选择,可以替代相对复杂的凹槽刻蚀工艺。
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引用次数: 5
Fabrication and Evaluation of Cassava Starch Acetate Nanoparticles Loaded with Drugs of Various BCS Classes: Influence of Drug Solubility and Partition Coefficient 负载不同BCS类药物的木薯醋酸淀粉纳米颗粒的制备与评价:药物溶解度和分配系数的影响
Pub Date : 2019-03-15 DOI: 10.4172/2324-8777.1000259
G. Paulos, T. Gebre-Mariam, Neubert Hhr
A successful fabrication of nanocarrier for drug delivery should yield nanoparticles (NPs) with suitable particle size and size distribution and provide high drug-loading capacity. Factors that influence these attributes include physicochemical properties of the drug, the nature of the nanocarrier, and processing variables, among others. The aim of this study was, therefore, to investigate the influence of solubility and partition coefficient of different drugs on the characteristics of starch-based NPs. Cassava starch was chemically modified by acetylation, at different degrees of substitution (DS) and characterized. The starch acetates (SAs) were then used for the preparation of drug-loaded NPs. Different model drugs: ibuprofen (BCS class II), acyclovir (BCS class III) and furosemide (BCS class IV) were incorporated into NPs using emulsification solvent evaporation technique. The effects of solubility and partition coefficient, and DS of SA on the properties of NPs, namely, size and size distribution, drug loading capacity (DL), encapsulation efficiency (EE) and in vitro release profile were investigated. The results showed that the DL and EE of ibuprofen and furosemide loaded starch acetate nanoparticles (SANPs) increased consistently with an increase in the DS of SA. On the contrary, DL and EE of acyclovir-loaded NPs decreased as DS of SA increased. Due to their poor solubility and high partition coefficient, the EEs of ibuprofen and furosemide in SANPs fabricated from SA with high DS were much greater than that of acyclovir. Furthermore, as DS of SA increased the cumulative release profile of Ibuprofen from SANPs was retarded whereas the release profile of acyclovir was enhanced. On the other hand, furosemide, the most lipophilic drug of all, exhibited lowest release profile over the study period of 8 h. In conclusion, along with the hydrophobic nature of SA, the DL, EE and drug release profile from SANPs depended on the solubility and partition coefficient of the incorporated drug molecule.
一种成功的药物递送纳米载体的制备,必须制备出具有合适粒径和粒径分布的纳米颗粒,并具有较高的载药能力。影响这些属性的因素包括药物的物理化学性质、纳米载体的性质和加工变量等。因此,本研究的目的是研究不同药物的溶解度和分配系数对淀粉基NPs特性的影响。对木薯淀粉进行了不同取代度的乙酰化改性,并对其进行了表征。然后将淀粉乙酸酯(SAs)用于制备载药NPs。不同的模型药物:布洛芬(BCS II类)、阿昔洛韦(BCS III类)和呋塞米(BCS IV类)采用乳化溶剂蒸发技术掺入NPs。考察了SA的溶解度、分配系数和DS对NPs的粒径和粒径分布、载药量(DL)、包封效率(EE)和体外释放特性的影响。结果表明,布洛芬和速尿负载的醋酸淀粉纳米颗粒(SANPs)的DL和EE随着SA的DS的增加而增加。相反,随着SA DS的增加,负载阿昔洛韦的NPs的DL和EE降低。由于布洛芬和呋塞米的溶解度差和分配系数高,在高DS的SA制备的SANPs中,其EEs远大于阿昔洛韦。此外,随着SA的DS的增加,布洛芬的累积释放谱被延缓,而阿昔洛韦的释放谱被增强。另一方面,速尿是所有药物中亲脂性最强的药物,在8 h的研究期间释放曲线最低。综上所述,除了SA的疏水性外,SANPs的DL、EE和药物释放曲线取决于掺入药物分子的溶解度和分配系数。
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引用次数: 1
New Perspectives on the Unique Micro and Nano-Structural Features of the Cu/ZnO Methanol Synthesis Catalyst Cu/ZnO甲醇合成催化剂独特微纳米结构特征的新研究
Pub Date : 2019-03-15 DOI: 10.4172/2324-8777.1000260
G. Mr.
The vapor phase methanol process, introduced by ICI technology in 1966, and the liquid phase methanol synthesis process (LPMeOHtm) introduced first by ChemSystems, Inc. (now Nexant) in 1975, are seen as the 2 big research/technology advances in the conventional methanol synthesis technology. The success of these 2 processes, both from a scientific and commercial standpoint, primarily is driven by the very superior, almost anomalous, performance of the proprietary Cu/ZnO/Al2O3ICI technical catalyst, and it’s very unique microstructural features, often termed as a “microcrystalline sponge”. The LPMeOHtm process overcomes some of the glaring drawbacks associated with the vapor phase process, viz., highly exothermal nature of methanol synthesis reactions, presence of local reactor hot spots which presents possibility of thermal runaways, and low per-pass CO/H2 conversions.
1966年由ICI技术推出的气相甲醇工艺和1975年由ChemSystems公司(现为Nexant)首次推出的液相甲醇合成工艺(LPMeOHtm)被视为传统甲醇合成技术的两大研究/技术进步。从科学和商业的角度来看,这两个过程的成功主要是由于专有的Cu/ZnO/Al2O3ICI技术催化剂的非常优越,几乎异常的性能,以及它非常独特的微观结构特征,通常被称为“微晶海绵”。LPMeOHtm工艺克服了与气相工艺相关的一些明显缺点,即甲醇合成反应的高度放热性质,存在可能出现热失控的局部反应器热点,以及每道CO/H2转化率低。
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引用次数: 0
Gas Sensing Properties of MoO3: NiO Nanocomposite Functionalized with Noble Metal towards Carbon Dioxide (CO2) 贵金属功能化MoO3: NiO纳米复合材料对二氧化碳的气敏性能
Pub Date : 2019-03-15 DOI: 10.4172/2324-8777.1000262
Manasa Mv, Devi Gs
In the present study we describe the design, fabrication and gas sensing performance of p-NiO/n-MoO3 (MN) nanocomposites functionalized by noble metal Pt (MNP). The formation of the nanocomposite was systematically reviewed and confirmed by X-Ray Fluorescence Spectroscopy (XRF) and X-Ray Diffraction (XRD) pattern. The MN nanocomposite impregnated with noble metal - Pt (MNP) showed better efficiency of S=92% towards Carbon dioxide (CO2) gas compared to MN (S=80) and selectivity towards CO2 in comparison to other interfering gases i.e., H2, EtOH, MeOH, NH3 and LPG, with superior stability.
本文研究了贵金属Pt (MNP)功能化p-NiO/n-MoO3 (MN)纳米复合材料的设计、制备及其气敏性能。通过x射线荧光光谱(XRF)和x射线衍射(XRD)对纳米复合材料的形成进行了系统的回顾和证实。与MN (S=80)相比,贵金属- Pt (MNP)浸染的MN纳米复合材料对二氧化碳(CO2)气体的效率为S=92%,对二氧化碳(CO2)气体的选择性优于其他干扰气体(H2, EtOH, MeOH, NH3和LPG),具有优越的稳定性。
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引用次数: 0
Study of the Dependency of pH Values on HAp Synthesis pH值对HAp合成影响的研究
Pub Date : 2019-03-15 DOI: 10.4172/2324-8777.1000258
M. Kamrujjaman, Kh., aker Ji, Haque Mm, R. Mo, Rahman Mm
Hydroxyapatite (Ca10(PO4)6(OH))2, HAp has been one of the cheapest and well-known ceramics for diversified applications including clinical bone graft procedures for more than 30 years. Synthetic calcium phosphates, such as calcium hydroxyapatite, are an important inorganic biomaterial which has attracted the attention of researchers related to the biomaterials field in recent years. HAp is widely used for hard tissues repair due to its chemical and structural similarity with the mineral phase of bone and teeth. As a result, this inorganic phosphate has been studied extensively for medical applications in the form of powders, composites, and coatings [1–11]. HAp has many bone replacement applications and is used as bone substitutes in dental and orthopedic sites, immediate tooth replacement, augmentation of alveolar ridges, pulp capping material and maxillofacial reconstruction, etc. [12]. HAp implants exhibit relatively good tissue compatibility, and new bone is formed directly on the implants [13-19]. For repairing or substituting the bone, the designed HAp material must have the ability to create a bond with the host living bone [20]. Hence, it is desirable to include a high degree of crystallinity and chemical stability among the desirable properties of an ideal hydroxyapatite [21-23] HAp has poor mechanical properties, e.g., low strength and toughness, restrict monolithic HAp applications to those that require little or no load-bearing parts [24]. Due to its diverse applications, the materials properties accordingly need to be tailored for an application. Hence, researchers have tried to customize its properties such as bioactivity, mechanical strength, solubility and sinter ability by controlling its composition, particle size and morphology [9,10]. The objectives of this work are to synthesize hydroxyapatite nanoparticles by chemical precipitation method for different pH value and to investigate the effects of the pH value variation during the reaction.
羟基磷灰石(Ca10(PO4)6(OH))2, HAp, 30多年来一直是最便宜和最知名的陶瓷之一,用于包括临床骨移植手术在内的各种应用。羟基磷灰石钙等合成磷酸钙是一种重要的无机生物材料,近年来引起了生物材料领域研究人员的广泛关注。羟基磷灰石由于其化学和结构与骨和牙齿的矿物相相似,被广泛用于硬组织修复。因此,这种无机磷酸盐已被广泛研究用于粉末、复合材料和涂料的医疗应用[1-11]。羟基磷灰石具有多种骨替代应用,可作为牙齿和骨科部位的骨替代物、即时牙齿替代、牙槽嵴增强、牙髓盖盖材料和颌面重建等。HAp种植体具有较好的组织相容性,新骨可直接在种植体上形成[13-19]。为了修复或替代骨,所设计的HAp材料必须具有与宿主活骨bb0建立连接的能力。因此,在理想羟基磷灰石的理想性能中,需要包括高结晶度和化学稳定性[21-23]。羟基磷灰石的机械性能较差,例如强度和韧性较低,这限制了单片羟基磷灰石的应用,只需要很少或不需要承重部件[24]。由于其应用的多样性,材料的特性需要根据不同的应用进行定制。因此,研究人员试图通过控制其组成、粒度和形态来定制其生物活性、机械强度、溶解度和烧结能力等特性[9,10]。采用化学沉淀法在不同的pH值下合成了羟基磷灰石纳米颗粒,并研究了pH值变化对反应的影响。
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引用次数: 1
Chitosan Nanoparticles as a Potential Drug Delivery System for Photodynamic Therapy of Cancer 壳聚糖纳米颗粒作为光动力治疗癌症的潜在药物递送系统
Pub Date : 2019-03-15 DOI: 10.4172/2324-8777.1000261
G. Amsaveni, M. Sakthivel, K. Kathiravan, B. Anish, R. Murugesan
Objective: Chitosan nanoparticles (CS-NP) can imbibe water insoluble anticancer agents into its hydrophobic multicores. In the present study, chitosan nanoparticles, a nanoscale drug carrier system is investigated for its potential as a drug delivery system for porphyrin based photodynamic therapy. Methods: Zinc meso tetra phenyl porphyrin (ZnmTPP) encapsulated CS-NP was prepared by ionic gelation method. The synthesized nanoparticles were characterized using dynamic light scattering studies, zeta potential analysis and AFM analysis. Results: Freshly prepared chitosan nanoparticles had an average hydrodynamic diameter of 175 nm and are nearly spherical in shape as per light scattering measurements and atomic force imaging respectively. As nanoscale drug carriers, (ZnmTPP) encapsulated chitosan nanoparticles exhibited high encapsulation efficiency and controlled release pattern. The encapsulated photosensitizer exhibited efficient singlet oxygen generation upon photo irradiation, retaining the photosensitization capacity of encapsulated hydrophobic ZnmTPP. The in vitro phototoxicities of free and nano-encapsulated ZnmTPP, studied using MTT assay in DLA cell lines demonstrate a concentration dependent response of photosensitizer in free and CS-nano formulations.
目的:壳聚糖纳米颗粒(CS-NP)可将不溶于水的抗癌药物吸收到其疏水性多核中。在本研究中,研究了壳聚糖纳米颗粒作为一种纳米级药物载体系统作为卟啉光动力药物递送系统的潜力。方法:采用离子凝胶法制备中位四苯基卟啉锌(ZnmTPP)包封CS-NP。采用动态光散射、zeta电位分析和原子力显微镜分析对合成的纳米颗粒进行了表征。结果:新制备的壳聚糖纳米粒子的平均水动力直径为175 nm,光散射测量和原子力成像结果表明,新制备的壳聚糖纳米粒子的形状接近球形。ZnmTPP包封壳聚糖纳米颗粒作为纳米级药物载体,具有较高的包封效率和控释模式。包封的光敏剂在光照射下表现出高效的单线态产氧,保留了包封的疏水性ZnmTPP的光敏能力。MTT法研究了游离和纳米包封ZnmTPP在DLA细胞系中的体外光毒性,结果表明,游离和纳米包封ZnmTPP的光敏剂具有浓度依赖性。
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引用次数: 1
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Journal of Nanomaterials & Molecular Nanotechnology
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