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alginate; n/a; heavy metals; high-speed counter-current chromatography (HSCCC); microwave processing; phytochemicals; microNIR; antioxidant activity; in-line monitoring; Wuyi Rock tea; metabolomics; seawater; optimization; walnut septum; color analysis; metabolite profiling; rosuvastatin; dispersive liquid-liquid microextraction; antioxidant; mouse melanoma B16 cells; nails; extraction; sample preparation; quality; MAE; Panax notoginseng; physicochemical properties; flow injection; ionic liquids; branched-chain keto acids; Semen Cuscutae; near-infrared spectroscopy; volatile organic compounds; odor; SFE; single-drop microextraction; experimental design; cluster analysis; therapeutic drug monitoring; Thymus algeriensis; metformin; tyrosinase; gas chromatography-olfactometry; Ajuga genevensis; phytosterols; serum; diabetes; GHB; polyphenols; ultrasound assisted extraction; microextraction; oolong tea; alkaloid; minor ginsenosides; inductively coupled plasma-mass spectrometry; wood; stir bar sorptive extraction; HPLC-Q-TOF/MS; GHB glucuronide; Hericium erinaceuns mycelium; endogenous values; cultivars; Tieguanyin tea cultivar; SIRT1; modification; HPLC-MS/MS; fluid bed process; steamed Panax notoginseng; dry extract; UPLC-QTOF MS; flavonoids; blood-enriching activity; UPLC-QqQ MS; HPLC-PDA; neurodegenerative disease; biological activity; rare earth elements; response surface methodology; solid-phase microextraction; Ultra-Turrax extraction; bovine hide; ultra-high-performance liquid chromatography tandem mass spectrometry; gel strength; hematopoiesis; genistein; muscle; Lycium ruthenicun; hemostatic activity; flavonoid; ultra-high-performance liquid chromatography coupled to electrospray ionization mass spectrometry; HILIC; surfactant; saponins; pigments; chlorogenic acids; daidzein; Fe3O4; LC-MS; Asphodeline lutea; actinidin; total polyphenolic content; stir cake sorptive extraction; gelatin; ruthenicunoid A