ABSTRACT
The current use of a single chemical component as the representative quality control marker of herbal food supplement is inadequate. In this CD80-Quantitative-Pattern-Activity-Relationship (QPAR) study, we built a bioactivity predictive model that can be applicable for complex mixtures. Through integrating the chemical fingerprinting profiles of the immunomodulating herb Radix Astragali (RA) extracts, and their related biological data of immunological marker CD80 expression on dendritic cells, a chemometric model using the Elastic Net Partial Least Square (EN-PLS) algorithm was established. The EN-PLS algorithm increased the biological predictive capability with lower value of RMSEP (11.66) and higher values of Rp2 (0.55) when compared to the standard PLS model. This CD80-QPAR platform provides a useful predictive model for unknown RA extract's bioactivities using the chemical fingerprint inputs. Furthermore, this bioactivity prediction platform facilitates identification of key bioactivity-related chemical components within complex mixtures for future drug discovery and understanding of the batch-to-batch consistency for quality clinical trials.
Subject(s)
B7-1 Antigen/biosynthesis , Drugs, Chinese Herbal/administration & dosage , Immunologic Factors/administration & dosage , Plant Extracts/administration & dosage , Astragalus propinquus , B7-1 Antigen/chemistry , Cell Line , Dendritic Cells/drug effects , Drug Discovery , Drugs, Chinese Herbal/chemistry , Gene Expression Regulation/drug effects , Humans , Immunologic Factors/chemistry , Plant Extracts/chemistry , Quantitative Structure-Activity RelationshipABSTRACT
INTRODUCTION: Isoflavones are main bioactive components of Pueraria lobata (Willd.) Ohwi. Puerarin has been used as the marker compound in herb quality evaluation in the Chinese Pharmacopoiea. However, it is also important to include the other isoflavones present in the herb, such as daidzin, daidzein, genistin and genistein, in the evaluation as they also contribute to the overall bioactivity of the herb. OBJECTIVE: To develop a rapid and reliable method for simultaneous quantitation of isoflavones for P. lobata herb quality evluation. METHODOLOGY: The chromatographic separation was performed on an Agilent rapid resolution liquid chromatographic system through gradient elution. The developed method for the quantification of puerarin, daidzin, daidzein, genistin and genistein was fully validated. When it was applied to analyse the extracts of P. lobata, baseline separation was obtained within 10 min. RESULTS: The amounts of puerarin, daidzin, daidzein and genistin varied greatly among the samples although their chromatographic fingerprints were similar to each other. The 19 samples studied were classified into three clusters (I-III) by principal component analysis based on the amounts of puerarin, daidzin, daidzein and genistin. CONCLUSION: The classification result can be related to herbal origins, but the classification outcome from the chromatographic fingerprinting similarity approach did not provide any geographical origin information. This shows that bioactive constituents can reflect the intrinsic quality of P. lobata more accurately.
Subject(s)
Isoflavones/chemistry , Principal Component Analysis , Pueraria/chemistry , Chromatography, Liquid/instrumentation , Chromatography, Liquid/methods , Chromatography, Liquid/standards , Geography , Limit of Detection , Plant Extracts/chemistry , Plant Extracts/classification , Quality ControlABSTRACT
Puerarin nanoparticles were firstly prepared in the process of solution-enhanced dispersion by supercritical CO(2) (SEDS) and then successfully microencapsulated by poly(l-lactide) (PLLA) in a modified SEDS process. By adding an organic non-solvent, an initial puerarin solution with a higher degree of saturation and lower concentration was obtained and applied in the SEDS process. The resulting puerarin nanoparticles were then suspended in PLLA solution and microencapsulated by PLLA in a modified SEDS process, where an 'injector' was employed in the particle suspension delivery system. The puerarin nanoparticles exhibited a good spherical shape, a smooth surface and a narrow particle size distribution with a mean particle size of 188 nm. After microencapsulation the puerarin-PLLA microparticles had a mean size of 675 nm, a drug load of 23.6% and an encapsulation efficiency of 39.4%; after a burst release at the first stage, the drug was released in a sustained process. Compared with the parallel study of a co-precipitation process, this microencapsulation process is a much more promising technique to prepare a drug-polymer carrier for a drug delivery system, especially for protein drugs.
Subject(s)
Biocompatible Materials/chemistry , Chromatography, Supercritical Fluid/methods , Drug Carriers/chemistry , Drug Compounding/methods , Isoflavones/chemistry , Nanoparticles/chemistry , Nanoparticles/ultrastructure , Polyesters/chemistry , Absorption , Capsules , Crystallization/methods , Diffusion , Isoflavones/administration & dosage , Materials Testing , Particle Size , Porosity , Surface Properties , Vasodilator Agents/administration & dosage , Vasodilator Agents/chemistryABSTRACT
The current approaches to the quality control of herbal medicines are either compound-oriented or pattern-oriented, the former targeting specific components with some known chemical properties and the latter targeting all detectable components. The marker approach uses specific chemical compounds with known molecular structures, while the multi-compound approach uses both chemical compounds with known structures and those with partial chemical information e.g. retention times, mass spectra and ultraviolet spectra. Apart from chromatographic techniques, new techniques such as oscillating and electrochemistry fingerprints have been developed for quality control. Chemometric resolution methods are widely used for component deconvolution and data comparison. Pattern recognition techniques are used for authentication of herbal medicines.
ABSTRACT
The three parts of Radix Angelicae Sinensis (Danggui) were reported to have different therapeutic effects. In order to investigate their chemical compositions of different parts of Danggui, gas chromatography-mass spectrometry (GC-MS) combined with chemometrics data analysis was applied to provide a more detailed study. Subwindow factor analysis (SFA) and a modified augmented evolving window orthogonal projection (AEWOP) method were used to resolve the batch GC-MS data sets from the Danggui samples. Then, t-test, Wilcoxon rank sum test, and principal component analysis (PCA) were applied to carry out the comparison job. The results indicate which components are found to have significant differences among the three parts. These findings may be helpful for further research of the pharmacological activities of Danggui.