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TEM (D) of MSNinitiator. Fig. 2 XPS of MSN (a)。 FM 464labeled endosomes (B)。 MSNinitiator (c) and MSNpolymer (M1) (d). Fig. 3 FTIR spectra of M1 (a)。 C for 2 days (center), and in cell culture medium supplemented with10% serum (right, red color due to cell medium). Unbound FluorPEG was dialyzed in the starting solution . Figure 2. Optical properties of SWNTbound FluorPEG. (a) Absorbance of FluorPEG/SWNT and free FluorPEG. Fig 2. (b) Corresponding fluorescence emission spectra. Fig 2. (c) Emission peak intensity of SWNT bound FluorPEG and free FluorPEG in a fluorescein concentration range of 200900 nM. Figure 3. pHdependent fluorescence and absorbance of FluorPEG/SWNT. Absorption curves of FluorPEG/SWNT at various pHs in the (a) fluorescein region (dashed line marks the peak at pH 12) . Figure 3. (b) SWNT region (curves are displaced for clarity). Figure 3. (c) Corresponding fluorescence emission spectra (236。 SEM (C) and TEM (D) of M2。 M3 (c) and MSNinitiator (d). Scheme 1 A schematic illustration of the surface functionalization for MSN and the fabrication of MSNpolymer. Fig. 4 SEM (A) and TEM (B) of M1。 《 材料研究方法 》 研究生課程 浙江工業(yè)大學(xué) 化工與材料學(xué)院 材料系 第 10章 綜合分析舉例 LiPing