CN105866064A - Method for rapidly measuring content of five saponins in radix-notoginseng medicinal materials with near infrared spectroscopy method and application - Google Patents
Method for rapidly measuring content of five saponins in radix-notoginseng medicinal materials with near infrared spectroscopy method and application Download PDFInfo
- Publication number
- CN105866064A CN105866064A CN201610284900.2A CN201610284900A CN105866064A CN 105866064 A CN105866064 A CN 105866064A CN 201610284900 A CN201610284900 A CN 201610284900A CN 105866064 A CN105866064 A CN 105866064A
- Authority
- CN
- China
- Prior art keywords
- radix
- ginseng
- near infrared
- notoginseng
- medicine
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 238000000034 method Methods 0.000 title claims abstract description 63
- 229930182490 saponin Natural products 0.000 title claims abstract description 55
- 150000007949 saponins Chemical class 0.000 title claims abstract description 55
- 238000004497 NIR spectroscopy Methods 0.000 title claims abstract description 11
- 235000017709 saponins Nutrition 0.000 title abstract description 49
- 239000000463 material Substances 0.000 title abstract description 23
- 239000001397 quillaja saponaria molina bark Substances 0.000 claims abstract description 46
- 238000001228 spectrum Methods 0.000 claims abstract description 21
- 238000002360 preparation method Methods 0.000 claims abstract description 19
- 238000004128 high performance liquid chromatography Methods 0.000 claims abstract description 12
- 238000004519 manufacturing process Methods 0.000 claims abstract description 12
- 241000180649 Panax notoginseng Species 0.000 claims abstract description 10
- 235000003143 Panax notoginseng Nutrition 0.000 claims abstract description 10
- 244000131316 Panax pseudoginseng Species 0.000 claims description 50
- 235000003181 Panax pseudoginseng Nutrition 0.000 claims description 48
- 238000002329 infrared spectrum Methods 0.000 claims description 21
- YURJSTAIMNSZAE-HHNZYBFYSA-N ginsenoside Rg1 Chemical compound O([C@@](C)(CCC=C(C)C)[C@@H]1[C@@H]2[C@@]([C@@]3(C[C@@H]([C@H]4C(C)(C)[C@@H](O)CC[C@]4(C)[C@H]3C[C@H]2O)O[C@H]2[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O2)O)C)(C)CC1)[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O YURJSTAIMNSZAE-HHNZYBFYSA-N 0.000 claims description 15
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims description 13
- 229930189092 Notoginsenoside Natural products 0.000 claims description 12
- YURJSTAIMNSZAE-UHFFFAOYSA-N UNPD89172 Natural products C1CC(C2(CC(C3C(C)(C)C(O)CCC3(C)C2CC2O)OC3C(C(O)C(O)C(CO)O3)O)C)(C)C2C1C(C)(CCC=C(C)C)OC1OC(CO)C(O)C(O)C1O YURJSTAIMNSZAE-UHFFFAOYSA-N 0.000 claims description 11
- 238000001514 detection method Methods 0.000 claims description 11
- 238000012360 testing method Methods 0.000 claims description 11
- FBFMBWCLBGQEBU-RXMALORBSA-N (2s,3r,4s,5s,6r)-2-[(2r,3r,4s,5s,6r)-2-[[(3s,5r,6s,8r,9r,10r,12r,13r,14r,17s)-3,12-dihydroxy-4,4,8,10,14-pentamethyl-17-[(2s)-6-methyl-2-[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyhept-5-en-2-yl]-2,3,5,6,7,9,11,12,13,15,16,17-dodecah Chemical compound O([C@@](C)(CCC=C(C)C)[C@@H]1[C@@H]2[C@@]([C@@]3(C[C@@H]([C@H]4C(C)(C)[C@@H](O)CC[C@]4(C)[C@H]3C[C@H]2O)O[C@H]2[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O2)O[C@H]2[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O2)O)C)(C)CC1)[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O FBFMBWCLBGQEBU-RXMALORBSA-N 0.000 claims description 9
- FBFMBWCLBGQEBU-GYMUUCMZSA-N 20-gluco-ginsenoside-Rf Natural products O([C@](CC/C=C(\C)/C)(C)[C@@H]1[C@H]2[C@H](O)C[C@H]3[C@](C)([C@]2(C)CC1)C[C@H](O[C@@H]1[C@H](O[C@H]2[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O2)[C@@H](O)[C@H](O)[C@@H](CO)O1)[C@H]1C(C)(C)[C@@H](O)CC[C@]31C)[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 FBFMBWCLBGQEBU-GYMUUCMZSA-N 0.000 claims description 9
- HYPFYJBWSTXDAS-UHFFFAOYSA-N Ginsenoside Rd Natural products CC(=CCCC(C)(OC1OC(CO)C(O)C(O)C1O)C2CCC3(C)C4CCC5C(C)(C)C(CCC5(C)C4CC(O)C23C)OC6OC(CO)C(O)C(O)C6OC7OC(CO)C(O)C(O)C7O)C HYPFYJBWSTXDAS-UHFFFAOYSA-N 0.000 claims description 9
- 235000005035 Panax pseudoginseng ssp. pseudoginseng Nutrition 0.000 claims description 9
- 235000003140 Panax quinquefolius Nutrition 0.000 claims description 9
- 235000008434 ginseng Nutrition 0.000 claims description 9
- 230000003595 spectral effect Effects 0.000 claims description 9
- UOJAEODBOCLNBU-UHFFFAOYSA-N vinaginsenoside R4 Natural products C1CC(C2(CC(O)C3C(C)(C)C(OC4C(C(O)C(O)C(CO)O4)OC4C(C(O)C(O)C(CO)O4)O)CCC3(C)C2CC2O)C)(C)C2C1C(C)(CCC=C(C)C)OC1OC(CO)C(O)C(O)C1O UOJAEODBOCLNBU-UHFFFAOYSA-N 0.000 claims description 9
- CBEHEBUBNAGGKC-UHFFFAOYSA-N ginsenoside Rg1 Natural products CC(=CCCC(C)(OC1OC(CO)C(O)C(O)C1O)C2CCC3(C)C2C(O)CC4C5(C)CCC(O)C(C)(C)C5CC(OC6OC(CO)C(O)C(O)C6O)C34C)C CBEHEBUBNAGGKC-UHFFFAOYSA-N 0.000 claims description 8
- UFNDONGOJKNAES-UHFFFAOYSA-N Ginsenoside Rb1 Natural products CC(=CCCC(C)(OC1OC(COC2OC(CO)C(O)C(O)C2O)C(O)C(O)C1O)C3CCC4(C)C3C(O)CC5C6(C)CCC(OC7OC(CO)C(O)C(O)C7OC8OC(CO)C(O)C(O)C8O)C(C)(C)C6CC(O)C45C)C UFNDONGOJKNAES-UHFFFAOYSA-N 0.000 claims description 7
- GZYPWOGIYAIIPV-JBDTYSNRSA-N ginsenoside Rb1 Chemical compound C([C@H]1O[C@H]([C@@H]([C@@H](O)[C@@H]1O)O)O[C@@](C)(CCC=C(C)C)[C@@H]1[C@@H]2[C@@]([C@@]3(CC[C@H]4C(C)(C)[C@@H](O[C@H]5[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O5)O[C@H]5[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O5)O)CC[C@]4(C)[C@H]3C[C@H]2O)C)(C)CC1)O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O GZYPWOGIYAIIPV-JBDTYSNRSA-N 0.000 claims description 7
- TXEWRVNOAJOINC-UHFFFAOYSA-N ginsenoside Rb2 Natural products CC(=CCCC(OC1OC(COC2OCC(O)C(O)C2O)C(O)C(O)C1O)C3CCC4(C)C3C(O)CC5C6(C)CCC(OC7OC(CO)C(O)C(O)C7OC8OC(CO)C(O)C(O)C8O)C(C)(C)C6CCC45C)C TXEWRVNOAJOINC-UHFFFAOYSA-N 0.000 claims description 7
- 238000007689 inspection Methods 0.000 claims description 6
- 230000008569 process Effects 0.000 claims description 6
- 239000000284 extract Substances 0.000 claims description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 4
- 238000002790 cross-validation Methods 0.000 claims description 4
- 238000011156 evaluation Methods 0.000 claims description 4
- 239000000843 powder Substances 0.000 claims description 4
- 239000000470 constituent Substances 0.000 claims description 3
- 230000008676 import Effects 0.000 claims description 3
- 239000000203 mixture Substances 0.000 claims description 3
- 238000010298 pulverizing process Methods 0.000 claims description 3
- 238000007781 pre-processing Methods 0.000 claims description 2
- 230000010354 integration Effects 0.000 claims 1
- 239000003814 drug Substances 0.000 abstract description 13
- 238000003908 quality control method Methods 0.000 abstract description 8
- 238000005516 engineering process Methods 0.000 abstract description 6
- 230000002159 abnormal effect Effects 0.000 abstract 1
- 239000004615 ingredient Substances 0.000 abstract 1
- 238000002203 pretreatment Methods 0.000 abstract 1
- 238000012795 verification Methods 0.000 abstract 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
- 238000010238 partial least squares regression Methods 0.000 description 9
- 241000208340 Araliaceae Species 0.000 description 8
- 239000012071 phase Substances 0.000 description 7
- 230000000857 drug effect Effects 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- PWAOOJDMFUQOKB-WCZZMFLVSA-N ginsenoside Re Chemical compound O[C@@H]1[C@H](O)[C@@H](O)[C@H](C)O[C@H]1O[C@H]1[C@H](O[C@@H]2[C@H]3C(C)(C)[C@@H](O)CC[C@]3(C)[C@@H]3[C@@]([C@@]4(CC[C@@H]([C@H]4[C@H](O)C3)[C@](C)(CCC=C(C)C)O[C@H]3[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O3)O)C)(C)C2)O[C@H](CO)[C@@H](O)[C@@H]1O PWAOOJDMFUQOKB-WCZZMFLVSA-N 0.000 description 5
- AOGZLQUEBLOQCI-UHFFFAOYSA-N ginsenoside-Re Natural products CC1OC(OCC2OC(OC3CC4(C)C(CC(O)C5C(CCC45C)C(C)(CCC=C(C)C)OC6OC(CO)C(O)C(O)C6O)C7(C)CCC(O)C(C)(C)C37)C(O)C(O)C2O)C(O)C(O)C1O AOGZLQUEBLOQCI-UHFFFAOYSA-N 0.000 description 5
- 239000000825 pharmaceutical preparation Substances 0.000 description 5
- 230000003285 pharmacodynamic effect Effects 0.000 description 5
- 238000004458 analytical method Methods 0.000 description 4
- 239000003153 chemical reaction reagent Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 238000012937 correction Methods 0.000 description 3
- 229940079593 drug Drugs 0.000 description 3
- 238000010828 elution Methods 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- 238000002347 injection Methods 0.000 description 3
- 239000007924 injection Substances 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 238000005070 sampling Methods 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 239000009692 xuesetong Substances 0.000 description 3
- 239000004677 Nylon Substances 0.000 description 2
- 208000007536 Thrombosis Diseases 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- OORMXZNMRWBSTK-LGFJJATJSA-N dammarane Chemical compound C1CCC(C)(C)[C@@H]2CC[C@@]3(C)[C@]4(C)CC[C@H]([C@H](C)CCCC(C)C)[C@H]4CC[C@@H]3[C@]21C OORMXZNMRWBSTK-LGFJJATJSA-N 0.000 description 2
- 239000012467 final product Substances 0.000 description 2
- 229930182470 glycoside Natural products 0.000 description 2
- 150000002338 glycosides Chemical class 0.000 description 2
- 238000002386 leaching Methods 0.000 description 2
- 239000007791 liquid phase Substances 0.000 description 2
- GBMDVOWEEQVZKZ-UHFFFAOYSA-N methanol;hydrate Chemical compound O.OC GBMDVOWEEQVZKZ-UHFFFAOYSA-N 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 229920001778 nylon Polymers 0.000 description 2
- SHCBCKBYTHZQGZ-CJPZEJHVSA-N protopanaxatriol Chemical compound C1C[C@H](O)C(C)(C)[C@@H]2[C@@H](O)C[C@@]3(C)[C@]4(C)CC[C@H]([C@@](C)(O)CCC=C(C)C)[C@H]4[C@H](O)C[C@@H]3[C@]21C SHCBCKBYTHZQGZ-CJPZEJHVSA-N 0.000 description 2
- BBEUDPAEKGPXDG-UHFFFAOYSA-N protopanaxatriol Natural products CC(CCC=C(C)C)C1CCC2(C)C1C(O)CC3C4(C)CCC(O)C(C)(C)C4C(O)CC23C BBEUDPAEKGPXDG-UHFFFAOYSA-N 0.000 description 2
- 238000012372 quality testing Methods 0.000 description 2
- 239000000344 soap Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- PYXFVCFISTUSOO-HKUCOEKDSA-N (20S)-protopanaxadiol Chemical compound C1C[C@H](O)C(C)(C)[C@@H]2CC[C@@]3(C)[C@]4(C)CC[C@H]([C@@](C)(O)CCC=C(C)C)[C@H]4[C@H](O)C[C@@H]3[C@]21C PYXFVCFISTUSOO-HKUCOEKDSA-N 0.000 description 1
- GHWSMQHJFMAATF-DSHMRAQASA-N 20(S)-protopanaxadiol Natural products CC(=CCC[C@@](O)(CO)[C@H]1CC[C@]2(C)[C@@H]1CC[C@H]3[C@@]2(C)CC[C@H]4C(C)(C)[C@@H](O)CC[C@]34CO)C GHWSMQHJFMAATF-DSHMRAQASA-N 0.000 description 1
- 239000003390 Chinese drug Substances 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 239000009277 Panax notoginseng extract Substances 0.000 description 1
- 238000003556 assay Methods 0.000 description 1
- PYXFVCFISTUSOO-UHFFFAOYSA-N betulafolienetriol Natural products C1CC(O)C(C)(C)C2CCC3(C)C4(C)CCC(C(C)(O)CCC=C(C)C)C4C(O)CC3C21C PYXFVCFISTUSOO-UHFFFAOYSA-N 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000013210 evaluation model Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000003306 harvesting Methods 0.000 description 1
- 230000023597 hemostasis Effects 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 230000000302 ischemic effect Effects 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 210000003205 muscle Anatomy 0.000 description 1
- 238000001320 near-infrared absorption spectroscopy Methods 0.000 description 1
- 238000004445 quantitative analysis Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000013558 reference substance Substances 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- 238000004611 spectroscopical analysis Methods 0.000 description 1
- 238000010183 spectrum analysis Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 229930182493 triterpene saponin Natural products 0.000 description 1
- 229910021642 ultra pure water Inorganic materials 0.000 description 1
- 239000012498 ultrapure water Substances 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
- 238000010200 validation analysis Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
- G01N21/17—Systems in which incident light is modified in accordance with the properties of the material investigated
- G01N21/25—Colour; Spectral properties, i.e. comparison of effect of material on the light at two or more different wavelengths or wavelength bands
- G01N21/31—Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry
- G01N21/35—Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry using infrared light
- G01N21/359—Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry using infrared light using near infrared light
Landscapes
- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Analytical Chemistry (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- General Physics & Mathematics (AREA)
- Immunology (AREA)
- Pathology (AREA)
- Investigating Or Analysing Materials By Optical Means (AREA)
Abstract
The invention relates to a method for rapidly measuring the content of five saponins in radix-notoginseng medicinal materials with the near infrared spectroscopy method and an application. The method includes the steps that different-batch radix notoginseng medicine materials are collected to compose a sample set, near infrared spectroscopy of the materials is collected, abnormal samples are eliminated, a calibration set and a verification set are divided, the suitable spectrum pretreatment method and suitable modeling wave bands are selected, the content of five-medicine-effect saponins in the radix-notoginseng medicinal materials is measured with the HPLC method to serve as the reference value, the chemometrics technology is applied, and a quantitative calibration model between the near infrared spectroscopy of the radix-notoginseng medicine materials and the content of the five-medicine-effect saponins of the radix-notoginseng medicine materials is built, and can be used for measuring the content of five medicine-effect saponins of unknown-content radix-notoginseng medicine materials and relative preparation production of the radix-notoginseng medicine materials. According to the method, the five medicine-effect saponins are main medicine-effect ingredients of a radix-notoginseng saponin preparation, and are similar to the quality control index of the five medicine-effect saponins; in this way, the rapid and efficient technology method can be provided for the quality control over the radix-notoginseng medicinal materials and the preparation of the radix-notoginseng medicinal materials, and the checking workload is reduced.
Description
Technical field
The present invention relates to five kinds of saponin content rapid assay methods in a kind of pseudo-ginseng, relate in particular to one
Plant and use near infrared spectroscopy quickly to measure the method for five kinds of drug effect saponin contents in pseudo-ginseng, belong to the traditional Chinese medical science
Medicine studying technological domain.
Background technology
Pseudo-ginseng is dry root and the root of Araliaceae plant Panax notoginseng (Burk) F.H.Chen
Stem, has the hemostasis of the scattered stasis of blood, effect of detumescence ding-tong, is a kind of important common Chinese medicine, goes up in China
Century-old use history.Wherein, the saponin component of pseudo-ginseng is considered as its Chinese drugs, with pseudo-ginseng
Total saposins is the traditional medicine Injectio of raw material, as " Xuesaitong Injection " and thrombus lead to, and annual sales amount the nearlyest 10,000,000,000, be
" cookle " of traditional Chinese medicine circle.
Pseudo-ginseng monomer saponin composition is mostly dammarane type (dammarane) tetracyclic triterpene saponin(e, can be divided into two
Big class, is 20 (S)-protopanaxadiol-type [20 (S)-protopanaxadiol] and 20 (S)-Protopanaxatriol types respectively
[20(S)-protopanaxatriol].Wherein notoginsenoside R, ginsenoside Rg1, ginsenoside Re, ginseng soap
Glycosides Rb1 and ginsenoside Rd are saponin components main in pseudo-ginseng, are proved to be pseudo-ginseng and the anti-cardiac muscle of preparation thereof
The main pharmacodynamics material of ischemic, is the index components of arasaponin class quality of the pharmaceutical preparations control.
Quality of medicinal material analysis is the source of tcm manufacturing process analysis and quality control.It is all pseudo-ginseng, no
The same place of production, different harvest time etc. all can cause the change of quality of medicinal material.Existing Saponins from Panax notoginseng
Content assaying method is mainly high efficient liquid phase analysis method, and the method wastes time and energy, and needs reference substance.Cause
This, it is quite necessary to set up the content assaying method of main pharmacodynamics material in pseudo-ginseng, with meet pseudo-ginseng and
The demand that its quality of the pharmaceutical preparations controls.
In near infrared spectrum (Near Infrared Spectroscopy, NIRS) energy reflected sample, organic molecule contains
The characteristic information of hydrogen group (such as C-H, N-H, O-H etc.).Near-infrared spectrum technique can be used for traditional Chinese medicine quality
Analyze, sample without or only need simple process, do not consume chemical reagent, simple to operate, quick, at Chinese medicine
Field of quality control has huge application potential.Near-infrared spectrum technique is combined chemometric techniques,
The quick detection of main pharmacodynamics material in pseudo-ginseng, to pseudo-ginseng and arasaponin class preparation
Quality control is significant.
Summary of the invention
It is an object of the invention to provide a kind of employing near infrared spectroscopy and quickly measure five kinds of medicines in pseudo-ginseng
The method of effect saponin content and application, control to provide quickly for pseudo-ginseng and the arasaponin class quality of the pharmaceutical preparations,
Efficient technical method, alleviates inspection workload.
It is an object of the invention to be achieved through the following technical solutions:
Near infrared spectroscopy is used quickly to measure the method for five kinds of saponin contents in pseudo-ginseng, including following step
Rapid:
1) collect the pseudo-ginseng of different batches or pseudo-ginseng extract or notoginseng preparations, obtain calibration set sample
This；
2) gather the near infrared spectrum data of described calibration set sample, use single order to lead filter method and pre-process,
Obtain feature near infrared spectrum data；
3) notoginsenoside R, ginsenoside Rg1, ginseng in described calibration set sample is measured by HPLC method
The content of saponin(e Re, ginsenoside Rb1 and ginsenoside Rd；
4) use PLS establishment step 2) described in the feature near infrared spectrum number of calibration set sample
According to step 3) described in quantitative calibration models between five kinds of saponin contents；
5) according to step 2) identical method gathers the near infrared spectrum data of testing sample, and it is described fixed to import
Amount calibration model, obtains five kinds of saponin contents of testing sample.
For ease of describing, by notoginsenoside R, ginsenoside Rg1, ginsenoside Re, ginseng in the present invention
Saponin(e Rb1 and ginsenoside Rd are referred to as five kinds of saponin(es.
In the present invention, sample collection be by collect the pseudo-ginseng of different batches or pseudo-ginseng extract or
Notoginseng preparations sample, to increase the representativeness of sample set." batch " alleged by the present invention is commonly used in the art one
Individual technical term, specific to the present invention, the difference between the medicinal material of different " batch " is embodied in: the place of production is (the most raw
Long environment), position, main root specification, collecting time, period of storage, arrival entry time, specification etc..
In order to preferably set up quantitative calibration models, the place of production of the present invention includes Wenshan Prefecture, Honghe, elder brother
The places of production such as bright city, Yuxi；Described position includes the positions such as pseudo-ginseng clip, main root, rib, fibrous root；Institute
State main root specification and include at least 10.
In the present invention, it is preferable that before carrying out near infrared spectra collection, sample is pre-processed: by pseudo-ginseng
Medicinal material sample is vacuum dried, and crosses 280 μm sieves, obtain pseudo-ginseng powder after pulverizing.
In the present invention, it is preferable that spectra collection mode is: integrating sphere diffusing reflection is sampled；Preferably pick-up slip
Part: wave-number range 4,000-10,000cm-1, scanning times 64 times, resolution ratio 4cm-1, reference spectrum is
Air.
In the present invention, it is preferable that use single order to lead filtering and spectrum is pre-processed.
In the present invention, it is preferable that the near infrared spectrum data gathered (is being included calibration set sample, is testing
Card collection sample and sample to be tested) pre-process before also include reject spectral singularity sample；It is further preferred that
Chauvenet inspection is used to reject spectral singularity sample.
In the present invention, it is preferable that use partial least-squares regression method (PLSR) to set up described quantitative correction mould
Type.
In the present invention, it is preferable that described five kinds of saponin constituents all with 4,000-10,000cm-1All band is built
Mould.
The present invention is after carrying out preferably spectroscopic data pretreatment and modeling wave band respectively, the most square with cross validation
Root error RMSECV is that index determines optimal number of principal components.Preferably, notoginsenoside R, ginsenoside
Rg1, ginsenoside Re, ginsenoside Rb1, the number of principal components of ginsenoside Rd be respectively 7,7,
7,7,8.
Preferably, step 4 of the present invention) in, also include the described quantitative calibration models set up is pre-
Survey the step that performance is evaluated；Described evaluation index includes coefficient R, predicted root mean square error
RMSEP；Further, if R value is close to 1, RMSEP value is the least, the most described quantitative calibration model
It is applicable to the detection of described testing sample；Otherwise, the most inapplicable.
Specifically, the step bag that the estimated performance of the described described quantitative calibration models to being set up is evaluated
Including: take above-mentioned five kinds of saponin contents known checking collection sample, according to step 2) identical method gathers to be measured
The near infrared spectrum data of sample, imports described quantitative calibration models, is verified five kinds of saponin(es of collection sample
Content；Compared with five kinds of true measured values of saponin content of checking collection sample, evaluation and foreca performance.
The detection of described checking collection five kinds of saponin contents of sample can use art methods, it is possible to uses above-mentioned
HPLC method.
Preferably, HPLC method chromatographic condition of the present invention: Agilent Zorbax SB-C18 chromatographic column；Stream
Dynamic phase: mobile phase A is water, flowing is B acetonitrile mutually；Gradient elution: 0～22min, 17%～19%B；
22～30min, 19%～27%B；30～35min, 27%B；35～47min, 27%～46%B；47～70
Min, 46%～90%B.
Specifically, HPLC method chromatographic condition of the present invention: Agilent Zorbax SB-C18 chromatographic column
(4.6 × 50mm, 1.8 μm)；Flowing phase: mobile phase A is water, flowing is B acetonitrile mutually；Gradient elution:
0～22min, 17%～19%B；22～30min, 19%～27%B；30～35min, 27%B；35～47min,
27%～46%B；47～70min, 46%～90%B；Detection wavelength 203nm；Sampling volume 3 μ L；Stream
Speed 0.8mL min-1；Column temperature 35 DEG C.
It is further preferred that the preparation of described HPLC method need testing solution includes: pseudo-ginseng shreds, and pulverizes,
Cross 280 μm sieves；Accurately weighed Notoginseng Root 0.5g, with 70% methanol-water (v/v) 40mL, ultrasonic (work
Frequency 53kHz) extract 1 hour；Filter, fully wash residue with 70% methyl alcohol, make to shift completely；60℃
Rotary evaporated to dryness；It is transferred in 5.0mL volumetric flask with 70% methyl alcohol, same solvent constant volume；Cross 0.22 μ
M nylon leaching film, to obtain final product.
Present invention additionally comprises above-mentioned employing near infrared spectroscopy and quickly measure five kinds of saponin contents in pseudo-ginseng
Method application in pseudo-ginseng, notoginseng preparations quality testing and control field.
Notoginseng preparations of the present invention includes XUESAITONG JIAONANG, Xuesaitong injection, XUESHUANTONG JIAONANG, thrombus
Logical injection etc..
Near-infrared spectral analysis technology is incorporated into five kinds of main saponins drug effects of pseudo-ginseng and preparation thereof by the present invention
In the detection of material, it is achieved that the quick mensuration to these five kinds of main pharmacodynamics materials, with traditional detection method
Compare, substantially reduce the testing time, save substantial amounts of manpower and materials.The present invention is conducive to improving pseudo-ginseng
Medicinal material and the quality of the pharmaceutical preparations thereof control level, can be in pseudo-ginseng detection and the production of arasaponin class preparation
Journey is promoted the use of.
The present invention is by the spectral band of five kinds of saponin(es in the near infrared spectrum of selection pseudo-ginseng sample, and extraction has
The characteristic spectrum wave band of effect, this feature spectral band has with the five kinds of saponin(es measured according to existing conventional method
Good correlation, can effectively monitor pseudo-ginseng and five kinds of saponin contents of preparation thereof.The present invention is by using
Spectral singularity sample is rejected in Chauvenet inspection, uses single order to lead filtering and pre-processes spectrum, with screening
Information, reduces noise, improves accuracy and the accuracy of the method detection.Five kinds of medicines involved in the present invention
Effect saponin(e is the main pharmacodynamics composition of arasaponin class preparation, and the Quality Control for arasaponin class preparation refers to
Mark thus can be that pseudo-ginseng and the quality of the pharmaceutical preparations thereof control to provide technical method fast and efficiently, alleviate inspection man
Measure.
Accompanying drawing explanation
Fig. 1 is that in experimental example 1, the near-infrared of pseudo-ginseng powder diffuses spectrogram；
The number of principal components of ginsenoside Rd's quantitative model and RMSECV graph of a relation in Fig. 2 experimental example 1；
Fig. 3 is five kinds of saponin(e model predication value figures relevant to reference value in experimental example 1.
Detailed description of the invention
Following example are used for illustrating the present invention, but are not limited to the scope of the present invention.Embodiment is not noted
Bright concrete technology or condition person, according to the technology described by the document in this area or condition, or according to product
Product specification is carried out.Agents useful for same or instrument unreceipted production firm person, be and can be purchased by regular channel
Available conventional products.
If no special instructions, following experimental example and embodiment instrument and reagent:
Antaris near infrared spectrometer (Thermo company, the U.S.), is equipped with integrating sphere diffusing reflection sampling apparatus
With RESULT 3.0 spectra collection software, the near infrared spectrum in collecting sample.
Agilent 1100 Series HPLC System (Agilent company, the U.S.), be furnished with quaternary solvent pump, from
Dynamic injector, column oven, variable wavelength UV-detector.Notoginsenoside R, ginsenoside Rg1, people
Ginseng saponin(e Re, ginsenoside Rb1 and five kinds of saponin(e standard items of ginsenoside Rd (upper Hiroad standing grain medical sci-tech
Development Co., Ltd, purity >=98%).
Liquid phase water is ultra-pure water (Millipore), chromatogram acetonitrile (Merck, Germany), and other reagent is for dividing
Analyse pure.
Experimental example 1
1 sample collection: take 173 groups of pseudo-ginseng different parts and (include pseudo-ginseng clip, main root, rib, fibrous root
At position), different sources (including the places of production such as Wenshan Prefecture, Honghe, Kunming, Yuxi), different big
The pseudo-ginseng sample of small dimension, vacuum drying, cross 280 μm sieves after pulverizing.
2 methods
2.1 measure five kinds of drug effect saponin contents in sample by HPLC method
2.1.1 prepared by need testing solution: accurately weighed Notoginseng Root 0.5g, with 70% methanol-water (v/v) 40mL,
Ultrasonic (operating frequency 53kHz) extracts 1 hour.Filter, fully wash residue with 70% methyl alcohol, made
Total transfer.Rotary evaporated to dryness at 60 DEG C.It is transferred in 5.0mL volumetric flask with 70% methyl alcohol, identical molten
Agent constant volume.Cross 0.22 μm nylon leaching film, to obtain final product.
2.1.2 chromatographic condition: Agilent Zorbax SB-C18 chromatographic column (4.6 × 50mm, 1.8 μm)；Stream
Dynamic phase water (A)-acetonitrile (B), gradient elution (0～22min, 17%～19%B；22～30min, 19%～27%
B；30～35min, 27%B；35～47min, 27%～46%B；47～70min, 46%～90%B)；
Detection wavelength 203nm；Sampling volume 3 μ L；Flow velocity 0.8mL min-1；Column temperature 35 DEG C.Bent according to standard
Five kinds of drug effect saponin contents in line computation pseudo-ginseng sample.
2.2 samples and near infrared spectra collection
Spectra collection condition: wave-number range 4,000-10,000cm-1, scanning times 64 times, resolution ratio 4cm-1,
Reference spectrum is air.The near-infrared of pseudo-ginseng powder diffuses spectrogram as shown in Figure 1.
3 results and discussion
3.1 near infrared spectrum data preprocess methods
Spectral singularity sample, then random division calibration set 152 example and checking is rejected according to Chauvenet inspection
Collect 16 examples.Using the modeling of all band PLSR, lead filtering with single order and pre-process spectrum, each saponin(e is all
Model for all band.Notoginsenoside R, ginsenoside Rg1, ginsenoside Re, ginsenoside Rb1 and people
The number of principal components of ginseng saponin(e Rd is respectively 7,7,7,7 and 8.
The method for building up of 3.2 quantitative calibration models
In order to remove the noise near infrared spectrum and interference.Use the modeling of all band PLSR, be respectively compared
Become without Pretreated spectra, first derivative, second dervative, multiplicative scatter correction (MSC) and standard canonical
Change (SNV) these five kinds of preprocessing procedures.Result is as shown in table 1-table 5, and result display single order leads filter
Ripple is preferable to five kinds of saponin(e quantitative results.Wherein RMSEC represents calibration set root-mean-square error；RMSEP table
Show forecast set root-mean-square error.
Table 1 R1 Pretreated spectra results contrast
Table 2 Rg1 Pretreated spectra results contrast
Table 3 Re Pretreated spectra results contrast
Table 4 Rb1 Pretreated spectra results contrast
Table 5 Rd Pretreated spectra results contrast
The selection of 3.3 spectral bands
Although PLSR method can to a certain degree eliminate the synteny of spectrum, still it is necessary modeling wave band is entered
Row optimizes.By comparing the modeling effect of different-waveband, the results are shown in Table 6-table 10.Five kinds of saponin(es are all entirely
Wave band modeling is more excellent.
Table 6 R1 wave band modeling effectiveness comparison
Table 7 Rg1 wave band modeling effectiveness comparison
Table 8 Re wave band modeling effectiveness comparison
Table 9 Rb1 wave band modeling effectiveness comparison
Table 10 Rd wave band modeling effectiveness comparison
The determination of 3.4 optimal number of principal components
Judge the number of principal components of PLSR according to cross validation root-mean-square error RMSECV, Fig. 2 is ginseng soap
The number of principal components of glycosides Rd quantitative model and cross validation root mean square residual (RMSECV) graph of a relation, when main one-tenth
When mark is 8, RMSECV tends towards stability.In like manner, the number of principal components of other saponin constituents is respectively as follows: R1,
7；Rg1,7；Re, 7；Rb1,7.
3.5 model prediction results
PLSR method is used to set up quantitative calibration models, with prediction related coefficient R and predicted root mean square error
RMSEP is metrics evaluation model prediction performance.
Use partial least-squares regression method (PLSR) by the NIR spectra of 152 example calibration set samples and HPLC
Five kinds of saponin contents that method records carry out returning association, set up the optimum near-infrared quantitative correction mould of five kinds of saponin(es
Type.By the near infrared spectrum input quantitative calibration models of remaining 16 example checking collection sample, calculate five kinds of saponin(es
Content, and compare with HPLC method measured value, with predicted root mean square error RMSEP for metrics evaluation mould
Type estimated performance, the RMSEP of notoginsenoside R, ginsenosides Rg1, Re and Rb1 and Rd is respectively
2.50,3.73,1.41,3.10 and 1.00.Relevant figure between predicted value and the reference value of each regression model
As shown in Figure 3.In Fig. 3, R1, Rg1, Re, Rb1, Rd represent notoginsenoside R, ginseng respectively
Saponin(e Rg1, ginsenoside Re, ginsenoside Rb1 and ginsenoside Rd；Calibration is calibration set,
Validation is checking collection.
Notoginsenoside R, ginsenosides Rg1, Re and Rb1 and the Rd prediction phase relation in calibration model
Number (R) is respectively 0.9463,0.9718,0.9347,0.9596 and 0.9892.
The application of 3.6 Quantitative Analysis Model
Under the conditions of selected Pretreated spectra and wave band, in pseudo-ginseng five kinds of drug effect saponin contents are carried out
Prediction.This pseudo-ginseng diffusing reflection near-infrared quantitative model, has higher precision of prediction, and five kinds of saponin(es become
The prediction related coefficient dividing (notoginsenoside R, ginsenosides Rg1, Re and Rb1 and Rd) is all higher than 0.93.
And Testing index is consistent with the quality control index of arasaponin class preparation, adds the practicality of method.Should
Method is suitable for by arasaponin class preparation production line feeding intake fast and accurately the content information of medicinal material, for system
The production of agent provides reference.Meanwhile, the method can be used for the quality testing of pseudo-ginseng acquisition phase.
Although, the present invention is described in detail the most with a general description of the specific embodiments,
But on the basis of the present invention, can make some modifications or improvements it, this is to those skilled in the art
Obviously.Therefore, these modifications or improvements without departing from theon the basis of the spirit of the present invention, all
Belong to the scope of protection of present invention.
Claims (10)
1. using near infrared spectroscopy quickly to measure the method for five kinds of saponin contents in pseudo-ginseng, its feature exists
In, comprise the following steps:
1) collect the pseudo-ginseng of different batches or pseudo-ginseng extract or notoginseng preparations, obtain calibration set sample
This；
2) gather the near infrared spectrum data of described calibration set sample, use single order to lead filter method and pre-process,
Obtain feature near infrared spectrum data；
3) notoginsenoside R, ginsenoside Rg1, ginseng in described calibration set sample is measured by HPLC method
The content of saponin(e Re, ginsenoside Rb1 and ginsenoside Rd；
4) use PLS establishment step 2) described in the feature near infrared spectrum number of calibration set sample
According to step 3) described in quantitative calibration models between five kinds of saponin contents；
5) according to step 2) identical method gathers the near infrared spectrum data of testing sample, and it is described fixed to import
Amount calibration model, obtains five kinds of saponin contents of testing sample.
Method the most according to claim 1, it is characterised in that described five kinds of saponin constituents all with 4,000
-10,000cm-1All band models.
Method the most according to claim 1 and 2, it is characterised in that spectra collection mode is: integration
Ball diffusing reflection is sampled；Acquisition condition: wave-number range 4,000-10,000cm-1, scanning times 64 times, differentiate
Rate 4cm-1, reference spectrum is air.
Method the most according to claim 1 and 2, it is characterised in that to the near infrared light gathered
Modal data also includes the step rejecting spectral singularity sample before pre-processing；Preferably, Chauvenet is used
Spectral singularity sample is rejected in inspection.
Method the most according to claim 1 and 2, it is characterised in that with cross validation root-mean-square error
RMSECV is that index determines optimal number of principal components；Preferably, notoginsenoside R, ginsenoside Rg1, people
Ginseng saponin(e Re, ginsenoside Rb1, the number of principal components of ginsenoside Rd be respectively 7,7,7,
7,8.
Method the most according to claim 1 and 2, it is characterised in that described step 4) in, also wrap
Include the step that the estimated performance to the quantitative calibration models set up is evaluated；Described evaluation index includes phase
Close coefficients R, predicted root mean square error RMSEP；Further, if R value is close to 1, RMSEP value
The least, the most described quantitative calibration model is applicable to the detection of described testing sample；Otherwise, the most inapplicable.
Method the most according to claim 1 and 2, it is characterised in that in described batch, the place of production includes literary composition
State, mountain, Honghe, Kunming, Yuxi；In described batch position include pseudo-ginseng clip, main root, rib,
Fibrous root；In described batch, main root specification includes at least 10.
Method the most according to claim 1 and 2, it is characterised in that carrying out near infrared spectra collection
Before sample is pre-processed: by pseudo-ginseng sample be vacuum dried, after pulverizing cross 280 μm sieve, obtain three
Seven medicinal powders.
Method the most according to claim 1 and 2, it is characterised in that described HPLC method chromatographic condition:
Agilent Zorbax SB-C18 chromatographic column；Flowing phase: mobile phase A is water, flowing is B acetonitrile mutually；Ladder
Degree wash-out: 0～22min, 17%～19%B；22～30min, 19%～27%B；30～35min, 27%B；
35～47min, 27%～46%B；47～70min, 46%～90%B.
10. the method described in any one of claim 1-9 is in pseudo-ginseng and the quality of arasaponin class preparation
Application in detection and control field.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201610284900.2A CN105866064A (en) | 2016-05-03 | 2016-05-03 | Method for rapidly measuring content of five saponins in radix-notoginseng medicinal materials with near infrared spectroscopy method and application |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201610284900.2A CN105866064A (en) | 2016-05-03 | 2016-05-03 | Method for rapidly measuring content of five saponins in radix-notoginseng medicinal materials with near infrared spectroscopy method and application |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN105866064A true CN105866064A (en) | 2016-08-17 |
Family
ID=56628890
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201610284900.2A Pending CN105866064A (en) | 2016-05-03 | 2016-05-03 | Method for rapidly measuring content of five saponins in radix-notoginseng medicinal materials with near infrared spectroscopy method and application |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN105866064A (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN106248620A (en) * | 2016-08-30 | 2016-12-21 | 辽宁上药好护士药业（集团）有限公司 | A kind of numbness preparation is dried the method for quick of intermediate multi objective |
| CN107153048A (en) * | 2017-06-12 | 2017-09-12 | 浙江大学 | The near infrared spectrum on-line detecting system and method for a kind of arasaponin column chromatography procedure |
| CN107727609A (en) * | 2017-09-27 | 2018-02-23 | 天津工业大学 | A kind of polynary based near infrared spectrum mixes pseudo- pseudo-ginseng quantitative analysis method |
| CN113740292A (en) * | 2021-10-11 | 2021-12-03 | 广东众生药业股份有限公司 | Quality control method for traditional Chinese medicine extraction process |
| CN116159770A (en) * | 2022-12-20 | 2023-05-26 | 浙江大学 | Chinese herbal medicine sorting robot and sorting method thereof |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102539566A (en) * | 2011-12-28 | 2012-07-04 | 河南中医学院 | Method for fast detecting content of dioscin in dioscorea zingiberensis by utilizing near infrared spectrum technology |
| CN103063605A (en) * | 2013-01-04 | 2013-04-24 | 云南植物药业有限公司 | Method for determining radix notoginseng extract and contents of five types of ginsenosides in preparation of radix notoginseng extract by Fourier transform near-infrared spectrograph |
| CN104062259A (en) * | 2013-05-06 | 2014-09-24 | 山东东阿阿胶股份有限公司 | Method for rapid determination of total saponin content in compound ass-hide glue pulp by near infrared spectroscopy |
-
2016
- 2016-05-03 CN CN201610284900.2A patent/CN105866064A/en active Pending
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102539566A (en) * | 2011-12-28 | 2012-07-04 | 河南中医学院 | Method for fast detecting content of dioscin in dioscorea zingiberensis by utilizing near infrared spectrum technology |
| CN103063605A (en) * | 2013-01-04 | 2013-04-24 | 云南植物药业有限公司 | Method for determining radix notoginseng extract and contents of five types of ginsenosides in preparation of radix notoginseng extract by Fourier transform near-infrared spectrograph |
| CN104062259A (en) * | 2013-05-06 | 2014-09-24 | 山东东阿阿胶股份有限公司 | Method for rapid determination of total saponin content in compound ass-hide glue pulp by near infrared spectroscopy |
Non-Patent Citations (5)
| Title |
|---|
| 杨南林 等: "中药材三七中皂苷类成分的近红外光谱快速无损分析新方法", 《化学学报》 * |
| 杨南林 等: "近红外光谱法快速测定三七总皂苷的方法研究", 《浙江大学学报（工学版）》 * |
| 郑丽华 等: "HPLC 测定三七总皂苷中5种皂苷的含量及稳定性考察", 《中医药临床杂志》 * |
| 闫珂巍 等: "近红外光谱法测定三七中3种皂苷的总含量", 《药物分析杂志》 * |
| 马雯霞: "高效液相色谱梯度洗脱法同时测定三七总皂苷中人参皂苷Rb1、人参皂苷Rg1和三七皂苷R1含量", 《中国药业》 * |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN106248620A (en) * | 2016-08-30 | 2016-12-21 | 辽宁上药好护士药业（集团）有限公司 | A kind of numbness preparation is dried the method for quick of intermediate multi objective |
| CN107153048A (en) * | 2017-06-12 | 2017-09-12 | 浙江大学 | The near infrared spectrum on-line detecting system and method for a kind of arasaponin column chromatography procedure |
| CN107727609A (en) * | 2017-09-27 | 2018-02-23 | 天津工业大学 | A kind of polynary based near infrared spectrum mixes pseudo- pseudo-ginseng quantitative analysis method |
| CN113740292A (en) * | 2021-10-11 | 2021-12-03 | 广东众生药业股份有限公司 | Quality control method for traditional Chinese medicine extraction process |
| CN116159770A (en) * | 2022-12-20 | 2023-05-26 | 浙江大学 | Chinese herbal medicine sorting robot and sorting method thereof |
| CN116159770B (en) * | 2022-12-20 | 2023-09-22 | 浙江大学 | Chinese herbal medicine sorting robot and sorting method thereof |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN105866064A (en) | Method for rapidly measuring content of five saponins in radix-notoginseng medicinal materials with near infrared spectroscopy method and application | |
| CN104048941B (en) | Method for quickly measuring content of multiple index components in radix ophiopogonis through near infrared spectroscopy | |
| CN103487395B (en) | A kind of Paris polyphylla medicinal material multiple index quick detecting method | |
| CN104062260B (en) | A kind of containing the near infrared online detection method in naringin Chinese Traditional Medicine | |
| CN109297929B (en) | Method for establishing quality grading of salvia miltiorrhiza decoction pieces by utilizing near infrared technology | |
| Zhu et al. | Simultaneous measurement of contents of liquirtin and glycyrrhizic acid in liquorice based on near infrared spectroscopy | |
| CN104792652A (en) | Multi-index rapid detection method for radix astragali | |
| CN108732126A (en) | A method of multicomponent content in red rooted salvia is measured using near infrared spectroscopy | |
| CN103063605A (en) | Method for determining radix notoginseng extract and contents of five types of ginsenosides in preparation of radix notoginseng extract by Fourier transform near-infrared spectrograph | |
| Shao et al. | Fast determination of two atractylenolides in Rhizoma Atractylodis Macrocephalae by Fourier transform near-infrared spectroscopy with partial least squares | |
| CN104568813A (en) | Multi-index fast detection method of dogwood medicinal materials | |
| CN104568822A (en) | Method for rapidly and simultaneously detecting multiple indexes of fructus forsythia medicinal material | |
| CN107449753A (en) | The method of rutin content near infrared spectrum quick test sophora flower processed product | |
| Zhang et al. | Multi critical quality attributes monitoring of Chinese oral liquid extraction process with a spectral sensor fusion strategy | |
| CN103411895B (en) | Pseudo-near infrared spectrum identification method mixed by pearl powder | |
| Wang et al. | Application of a data fusion strategy combined with multivariate statistical analysis for quantification of puerarin in Radix puerariae | |
| CN108562556A (en) | A kind of near infrared spectrum detection method of campanulaceae medicinal material | |
| Li et al. | Online near-infrared analysis coupled with MWPLS and SiPLS models for the multi-ingredient and multi-phase extraction of licorice (Gancao) | |
| CN108663337A (en) | A kind of method and its application measuring tanshinone component | |
| Fan et al. | Quality assessment of Fritillariae cirrhosae using portable NIR spectrometer | |
| CN105784951A (en) | Multiple indicator rapid detection method for raw medicinal powder of condensed pill of six drugs with rehmannia | |
| CN102759591B (en) | The detection method of content of 10 kinds of ginsenosides in a kind of injection Yiqi and vein recovery | |
| CN107643343B (en) | HPLC fingerprint spectrum determination method of Yunv Jian standard soup | |
| Han et al. | Rapid analysis of the in-process extract solutions of compound E Jiao oral liquid using near infrared spectroscopy and partial least-squares regression | |
| CN107807190A (en) | A kind of HPLC methods of 3 kinds of active components in measure hymsleya amabilis |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| TA01 | Transfer of patent application right | ||
| TA01 | Transfer of patent application right |
Effective date of registration: 20170714 Address after: 150060 Heilongjiang city of Harbin province Harbin Development Zone Road haping road centralized District No. 8 Yantai Applicant after: Haerbin Zhenbao Pharmaceutical Co., Ltd. Applicant after: Heilongjiang ZBD Pharmaceutical Co., Ltd. Address before: 150060 Heilongjiang city of Harbin province Harbin Development Zone Road haping road centralized District No. 8 Yantai Applicant before: Haerbin Zhenbao Pharmaceutical Co., Ltd. |
|
| RJ01 | Rejection of invention patent application after publication | ||
| RJ01 | Rejection of invention patent application after publication |
Application publication date: 20160817 |