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DOI 10.2174/1386207321666180913113803

Медицинская библиотека · Combinatorial chemistry & high throughput screening · 2018

Structural Characterization of Gallbladder Stones Using Energy Dispersive X-ray Spectroscopy and X-ray Diffraction.

Almarshad Hassan A, Badawy Sayed M, Alsharari Abdalkarem F

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

AIM AND

OBJECTIVE

Formation of the gallbladder stones is a common disease and a major health problem. The present study aimed to identify the structures of the most common types of gallbladder stones using X-ray spectroscopic techniques, which provide information about the process of stone formation.

MATERIAL AND METHOD: Phase and elemental compositions of pure cholesterol and mixed gallstones removed from gallbladders of patients were studied using energy-dispersive X-ray spectroscopy combined with scanning electron microscopy analysis and X-ray diffraction.

RESULTS

The crystal structures of gallstones which coincide with standard patterns were confirmed by X-ray diffraction. Plate-like cholesterol crystals with laminar shaped and thin layered structures were clearly observed for gallstone of pure cholesterol by scanning electron microscopy; it also revealed different morphologies from mixed cholesterol stones. Elemental analysis of pure cholesterol and mixed gallstones using energy-dispersive X-ray spectroscopy confirmed the different formation processes of the different types of gallstones.

CONCLUSION

The method of fast and reliable X-ray spectroscopic techniques has numerous advantages over the traditional chemical analysis and other analytical techniques. The results also revealed that the X-ray spectroscopy technique is a promising technique that can aid in understanding the pathogenesis of gallstone disease.

Для цитирования: Almarshad Hassan A, Badawy Sayed M, Alsharari Abdalkarem F. Structural Characterization of Gallbladder Stones Using Energy Dispersive X-ray Spectroscopy and X-ray Diffraction.. Combinatorial chemistry & high throughput screening. 2018. DOI: 10.2174/1386207321666180913113803.

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