Detection of minute chemical species by principal component analysis

被引:43
作者
Hasegawa, T [1 ]
机构
[1] Kobe Pharmaceut Univ, Higashinada Ku, Kobe, Hyogo 6588558, Japan
关键词
D O I
10.1021/ac981430z
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A novel analytical technique based on the detection of minute bands in a mixture spectrum with the use of principal-component analysis (PCA) is presented. This new aspect of PCA indicates that overlapped spectra of some components can be separated with no a priori knowledge of the components when the absorbances of the components vary greatly. This technique can be used for the detection of minute chemical species. The concept was confirmed by computer simulations. In the simulations, abstract spectra (loading vectors) were successfully obtained, and the changes of the component absorbances were also successfully followed semiquantitatively by calculating their scores. The method developed with PCA was applied to the analysis of infrared reflection-absorption (RA) spectra to study molecular interaction mechanism between alkyl-deuterated dipalmitoylphosphatidylcholine (DPPC-d(62)) monolayer and sucrose. The samples were Langmuir-Blodgett (LB) films of the DPPC-d(62) monolayer that was prepared on a sucrose solution. The LB films consisted of the following phases: air/DPPC-d(62) + sucrose/sucrose/substrate (gold). The abstract spectra corresponding to "DPPC-d(62) + sucrose" and "sucrose" phases were successfully separated by PCA, and the absorbance change of sucrose in each phase was semiquantitatively calculated from the score. The absorbance change was experimentally confirmed with quartz-crystal microbalance (QCM) experiments. In addition, minute water molecules that remained in the LB films after drying were readily detected from an abstract spectrum, and their binding site was found to be the phospholipid moiety in the head group of DPPC-d(62).
引用
收藏
页码:3085 / 3091
页数:7
相关论文
共 40 条
[1]  
[Anonymous], 1970, SYM FARADAY SOC
[2]   Predictions of secondary structure using statistical analyses of electronic and vibrational circular dichroism and Fourier transform infrared spectra of proteins in H2O [J].
Baumruk, V ;
Pancoska, P ;
Keiderling, TA .
JOURNAL OF MOLECULAR BIOLOGY, 1996, 259 (04) :774-791
[3]   Monomolecular films of fatty acids on glass [J].
Blodgett, KB .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1934, 56 :495-495
[4]   A GENERALIZED-APPROACH TO DERIVATIVE SPECTROSCOPY [J].
CAMERON, DG ;
MOFFATT, DJ .
APPLIED SPECTROSCOPY, 1987, 41 (04) :539-544
[5]   INTERACTIONS OF SUGARS WITH MEMBRANES [J].
CROWE, JH ;
CROWE, LM ;
CARPENTER, JF ;
RUDOLPH, AS ;
WISTROM, CA ;
SPARGO, BJ ;
ANCHORDOGUY, TJ .
BIOCHIMICA ET BIOPHYSICA ACTA, 1988, 947 (02) :367-384
[6]   2D FT-NIR and FT-IR correlation analysis of temperature-induced changes of nylon 12 [J].
Czarnecki, MA ;
Wu, PY ;
Siesler, HW .
CHEMICAL PHYSICS LETTERS, 1998, 283 (5-6) :326-332
[7]   ACYL CHAIN PACKING PROPERTIES OF DEUTERATED LIPID BILAYER DISPERSIONS - VIBRATIONAL RAMAN SPECTRAL PARAMETERS [J].
DEVLIN, MT ;
LEVIN, IW .
JOURNAL OF RAMAN SPECTROSCOPY, 1990, 21 (07) :441-451
[9]   SUCCESSIVE AVERAGE ORTHOGONALIZATION OF SPECTRAL DATA [J].
DONAHUE, SM ;
BROWN, CW .
ANALYTICAL CHEMISTRY, 1991, 63 (10) :980-985
[10]   QUANTITATIVE 2-DIMENSIONAL INFRARED (2D IR) SPECTROSCOPY - THEORETICAL DEVELOPMENT FOR GENERAL AND SPECIFIC CASES [J].
EKGASIT, S ;
ISHIDA, H .
APPLIED SPECTROSCOPY, 1995, 49 (09) :1243-1253