XÁC ĐỊNH PARACETAMOL TRONG MẪU DƯỢC PHẨM BẰNG PHƯƠNG PHÁP PHỔ HẤP THỤ PHÂN TỬ UV-VIS SỬ DỤNG HIỆN TƯỢNG CỘNG HƯỞNG PLASMON BỀ MẶT CỦA DUNG DỊCH NANO VÀNG

Lê Phương Thảo1, Nguyễn Thị Nguyệt1, Phạm Thị Ngọc Mai1
1 Khoa Hoá học, Trường Đại học Khoa học Tự nhiên, Đại học Quốc gia Hà Nội

Nội dung chính của bài viết

Tóm tắt

DETERMINATION OF PARACETAMOL IN PHARMACEUTICAL SAMPLES BY UV-VIS SPECTROPHOTOMETRIC METHOD USING SURFACE PLASMON RESONANCE (SPR) OF NANO GOLD SOLUTION

A highly sensitive molecular absorption UV-VIS method has been developed for the measurement of paracetamol in drug samples, based on the change in surface plasmon resonance (SPR) properties of gold nano particles in the presence of paracetamol. Visual detection of paracetamol trace in nano gold particle solution is possible through color change of solution from red to blue. The optical absorption ratio A690/A520 increases linearly with logarithm of paracetamol concentration in the range 5×10-7 M - 2.5×10-5 M. At the optimum conditions including 0.038 M NaCl, pH 4 with incubation time of 17 minutes, the developed method has very low limit of detection (LOD) of 1.61×10-7 M, relative standard deviation %RSD < 5%. The influence of possible coexisting subtances (Na2CO3, caffeine, dextromethorphan) in the drug samples is negligible (%S < 6%). The colorimetric method was successfully applied for the determination of paracetamol in serveral drug samples.

Chi tiết bài viết

Tài liệu tham khảo

1. Mouayed Q. Al-Abachi, Sarria A. Al-Safi, Hind S. Al-Ward, Spectrophotometric kinetic methods for the determination of paracetamol in pure form and pharmaceutical preparations, Iraqi Journal of Science, 2015, 56:2704-2717.
2. Mallah M.A., Sherazi S.T., Bhanger M.I., Mahesar S.A., Bajeer M.A., A rapid Fourier-transform infrared (FTIR) spectroscopic method for direct quantification of paracetamol content in solid pharmaceutical formulations, Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 2015, 141:64-70.
3. Mahesh Attimarad, Simultaneous determination of paracetamol and lornoxicam by RP-HPLC in bulk and tablet formulation, Pharmaceutical Methods, 2011, 2(1):61-66.
4. Tânia A.P. Fernandes, Joãn P. Aguiara, Ana I. Fernandesa, João F. Pintob, Quantification of theophylline or paracetamol in milk matrices by high-performance liquid chromatography, Journal of Pharmaceutical Analysis, 2017, 7(6):401-405.
5. Sonia Di Berardino, Renata Jinationowska, Rapid and sensitive CZE method for quality control analysis of pharmaceuticals containing pseudoephedrine, triprolidine and paracetamol, American Journal of Analytical Chemistry, 2014, 5(9):613-619.
6. Bohnenstengel F., Kroemer H.K., Sperker B., In vitro cleavage of paracetamol glucuronide by human liver and kidney β-glucuronidase: determination of paracetamol by capillary electrophoresis, Journal of Chromatography B: Biomedical Sciences and Applications, 1999, 721(2):295-299.
7. Nguyễn Vân Trang, Dương Minh Ngọc, Nguyễn Thùy Linh, Nguyễn Hoài Thu, Phạm Tiến Đức, Nguyễn Thị Ánh Hường, Phạm Thị Ngọc Mai, Xác định hàm lượng cysteine trong thực phẩm chức năng bằng phương pháp UV-Vis sử dụng hạt nano vàng, Tạp chí Phân tích Hóa, Lý và Sinh học, 2018, 23(5):39-44.
8. AOAC, Appendix F: Guidelines for standard method performance requirements, AOAC official methods of Analysis, 2012.