Chinese Journal of Chromatography ›› 2026, Vol. 44 ›› Issue (8): 889-899.DOI: 10.3724/SP.J.1123.2025.08024
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LIU Junyi1, ZHENG Yi1,2, YAN Jingyu1,2,*(
)
Received:2025-08-30
Online:2026-08-08
Published:2026-07-30
Supported by:CLC Number:
LIU Junyi, ZHENG Yi, YAN Jingyu. Research advances in the preparation and structural characterization of depolymerized oligosaccharides from traditional Chinese medicine[J]. Chinese Journal of Chromatography, 2026, 44(8): 889-899.
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URL: https://www.chrom-china.com/EN/10.3724/SP.J.1123.2025.08024
| Comparison of degradation methods | Acid hydrolysis | Oxidative degradation | Enzymatic hydrolysis | Assisted degradation |
|---|---|---|---|---|
| Core mechanism | electrophilic attack of H⁺ on the glycosidic oxygen atom | non-specific attack by ROS (e.g., ·OH) on glycosidic bonds and sugar rings | highly specific recognition and cleavage of target glycosidic bonds | enhancement of mass transfer and reaction efficiency via physical fields or novel solvents |
| Specificity | non-specific cleavage of all acid-labile bonds | non-specific | highly specific to certain linkage types and sugar units | inherits the specificity of the primary degradation method |
| Condition mildness | high temperature and strong acid required | relatively mild; special equipment for ozone | typically under mild conditions | can lower the required temperature or time of the core reaction |
| Product controllability | mixture with a broad DP range, low controllability | preliminary control of degradation extent | can directionally produce oligosaccharides of specific DP | significantly improves the controllability of the core method |
| Main by-products/effects | 5-HMF, furfural, monosaccharides, monosaccharide degradation | uronic acid loss; sugar ring opening; aldehyde/carboxyl group introduction | few side reactions, pure products | generally reduced; milder conditions reduce secondary degradation |
| Structural destructiveness | dehydration; configuration change due to harsh conditions | hydroxyl oxidation; C-C bond cleavage | perfectly preserves sugar ring structures and configurations | aims to mitigate the destructiveness of the core method |
| Environmental friendliness | strong acid usage; waste acid streams | H₂O₂ decomposes to H₂O; expensive periodate | green process, mild conditions, no hazardous waste | improved efficiency leads to greener processes |
| Typical application | initial depolymerization, large-scale pretreatment, sample prep for analysis | producing antioxidant oligosaccharides, structural sequencing, material modification | directed preparation of well-defined oligosaccharides for detailed SAR studies | enhanced efficiency of traditional methods |
Table 1 Comparison of major degradation methods for polysaccharides from traditional Chinese medicine
| Comparison of degradation methods | Acid hydrolysis | Oxidative degradation | Enzymatic hydrolysis | Assisted degradation |
|---|---|---|---|---|
| Core mechanism | electrophilic attack of H⁺ on the glycosidic oxygen atom | non-specific attack by ROS (e.g., ·OH) on glycosidic bonds and sugar rings | highly specific recognition and cleavage of target glycosidic bonds | enhancement of mass transfer and reaction efficiency via physical fields or novel solvents |
| Specificity | non-specific cleavage of all acid-labile bonds | non-specific | highly specific to certain linkage types and sugar units | inherits the specificity of the primary degradation method |
| Condition mildness | high temperature and strong acid required | relatively mild; special equipment for ozone | typically under mild conditions | can lower the required temperature or time of the core reaction |
| Product controllability | mixture with a broad DP range, low controllability | preliminary control of degradation extent | can directionally produce oligosaccharides of specific DP | significantly improves the controllability of the core method |
| Main by-products/effects | 5-HMF, furfural, monosaccharides, monosaccharide degradation | uronic acid loss; sugar ring opening; aldehyde/carboxyl group introduction | few side reactions, pure products | generally reduced; milder conditions reduce secondary degradation |
| Structural destructiveness | dehydration; configuration change due to harsh conditions | hydroxyl oxidation; C-C bond cleavage | perfectly preserves sugar ring structures and configurations | aims to mitigate the destructiveness of the core method |
| Environmental friendliness | strong acid usage; waste acid streams | H₂O₂ decomposes to H₂O; expensive periodate | green process, mild conditions, no hazardous waste | improved efficiency leads to greener processes |
| Typical application | initial depolymerization, large-scale pretreatment, sample prep for analysis | producing antioxidant oligosaccharides, structural sequencing, material modification | directed preparation of well-defined oligosaccharides for detailed SAR studies | enhanced efficiency of traditional methods |
| Chromatography technique | Stationary phase | Main advantages | Typical application scenarios | Application cases | Ref. |
|---|---|---|---|---|---|
| GPC/SEC | porous particles | enables separation by molecular size/hydrodynamic volume; mild conditions | fractionation by degree of polymerization; desalting; removal of large/small molecules | isolation and purification of oligosaccharides produced by hydrolysis of oat β-glucan | [ |
| IEC | charged functional groups (e.g., DEAE, CM) | high capacity for charged molecules; achieves separation by charge density/properties | separation of acidic/charged oligosaccharides; often serves as the first purification step | separation of hydrolyzed oligosaccharides from Plantago major L. | [ |
| HILIC | polar groups | exhibits superior performance for polar compounds; high resolution for isomers | separation of neutral/ polar oligosaccharides and isomers; often coupled with MS | separation of native cello-oligosaccharides and oxidized cello-oligosaccharides produced by cellulose hydrolysis | [ |
| PGC | porous graphitized carbon | exceptional resolution for isomers; maintains stability under wide pH range | separation of challenging isomeric oligosaccharides for detailed structural analysis | separation and analysis of oligosaccharides from multiple sources | [ |
Table 2 Summary of the applicability of different separation and purification techniques
| Chromatography technique | Stationary phase | Main advantages | Typical application scenarios | Application cases | Ref. |
|---|---|---|---|---|---|
| GPC/SEC | porous particles | enables separation by molecular size/hydrodynamic volume; mild conditions | fractionation by degree of polymerization; desalting; removal of large/small molecules | isolation and purification of oligosaccharides produced by hydrolysis of oat β-glucan | [ |
| IEC | charged functional groups (e.g., DEAE, CM) | high capacity for charged molecules; achieves separation by charge density/properties | separation of acidic/charged oligosaccharides; often serves as the first purification step | separation of hydrolyzed oligosaccharides from Plantago major L. | [ |
| HILIC | polar groups | exhibits superior performance for polar compounds; high resolution for isomers | separation of neutral/ polar oligosaccharides and isomers; often coupled with MS | separation of native cello-oligosaccharides and oxidized cello-oligosaccharides produced by cellulose hydrolysis | [ |
| PGC | porous graphitized carbon | exceptional resolution for isomers; maintains stability under wide pH range | separation of challenging isomeric oligosaccharides for detailed structural analysis | separation and analysis of oligosaccharides from multiple sources | [ |
| Technique | Primary analytical scope | Core advantages | Major limitations |
|---|---|---|---|
| Monosaccharide composition analysis | qualitative/quantitative analysis of monosaccharide types and molar ratios | high sensitivity; provides fundamental primary information for structural elucidation | prone to monosaccharide degradation during acid hydrolysis; no glycosidic linkage/sequence information |
| MS | molecular weight determination; molecular formula inference; sequence/partial linkage elucidation | extremely high sensitivity, minimal sample consumption; detailed fragment ion information; compatibility with LC/GC for analyzingcomplex mixtures | limited distinction of isomeric monosaccharides; difficult linkage differentiation via isobaric fragments; no α/β anomeric configuration information; quantitative accuracy dependent on ionization efficiency |
| Methylation analysis | glycosidic linkage position/branching point identification; hydroxyl group involvement in linkages | recognized as authoritative for direct linkage determination; clear branching architecture revelation; intuitive results comparable with standard libraries | complex; lengthy; multi-step derivatization; ineffective for acidic/sulfate-containing oligosaccharides; destructive to analytes; no sequence/anomeric configuration information |
| NMR spectroscopy | complete molecular structure elucidation; α/β anomeric configuration; sugar ring conformation; linkage sequence; branch point location | provides complete solution-phase stereochemical and conformational information | requires high-purity, milligram-scale samples; complex spectrum interpretation due to severe signal overlap |
Table 3 Comparison of four key technologies for oligosaccharide structural analysis
| Technique | Primary analytical scope | Core advantages | Major limitations |
|---|---|---|---|
| Monosaccharide composition analysis | qualitative/quantitative analysis of monosaccharide types and molar ratios | high sensitivity; provides fundamental primary information for structural elucidation | prone to monosaccharide degradation during acid hydrolysis; no glycosidic linkage/sequence information |
| MS | molecular weight determination; molecular formula inference; sequence/partial linkage elucidation | extremely high sensitivity, minimal sample consumption; detailed fragment ion information; compatibility with LC/GC for analyzingcomplex mixtures | limited distinction of isomeric monosaccharides; difficult linkage differentiation via isobaric fragments; no α/β anomeric configuration information; quantitative accuracy dependent on ionization efficiency |
| Methylation analysis | glycosidic linkage position/branching point identification; hydroxyl group involvement in linkages | recognized as authoritative for direct linkage determination; clear branching architecture revelation; intuitive results comparable with standard libraries | complex; lengthy; multi-step derivatization; ineffective for acidic/sulfate-containing oligosaccharides; destructive to analytes; no sequence/anomeric configuration information |
| NMR spectroscopy | complete molecular structure elucidation; α/β anomeric configuration; sugar ring conformation; linkage sequence; branch point location | provides complete solution-phase stereochemical and conformational information | requires high-purity, milligram-scale samples; complex spectrum interpretation due to severe signal overlap |
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