Functionalised nanoformulation of Swertiamarin with enhanced stability and hemocompatibility: synthesis, characterisation and anticancer evaluation
This study aimed to enhance the stability and compatibility of swertiamarin by loading it on amino-functionalised graphene oxide (GO) by ultrasonication. The nanoformulation showed a new peak in the FTIR spectrum (1658 cm −1 ) and a coupled peak in the UV-Vis spectrum implying CO-NH 2 interaction be...
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Published in | Materials technology (New York, N.Y.) Vol. 36; no. 7; pp. 440 - 449 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
Taylor & Francis
07.06.2021
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Abstract | This study aimed to enhance the stability and compatibility of swertiamarin by loading it on amino-functionalised graphene oxide (GO) by ultrasonication. The nanoformulation showed a new peak in the FTIR spectrum (1658 cm
−1
) and a coupled peak in the UV-Vis spectrum implying CO-NH
2
interaction between swertiamarin and functionalised GO. The SEM image revealed a sheet-like appearance with an average particle size of 252.38 ± 86.09 nm. The nanoformulation was non-haemolytic at 200 μg/mL (<5%) whereas swertiamarin was haemolytic at 50 μg/mL concentration. The freeze-dried samples exhibited good stability at normal storage condition. The formulation and the swertiamarin displayed similar anticancer activity against HepG2 cell lines with an average IC
50
value of 110 ± 0.75 μg/mL, respectively. Hence, the functionalised GO can be considered as a compatible carrier for bioactive compounds which provides better hemocompatibility and stability. |
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AbstractList | This study aimed to enhance the stability and compatibility of swertiamarin by loading it on amino-functionalised graphene oxide (GO) by ultrasonication. The nanoformulation showed a new peak in the FTIR spectrum (1658 cm
−1
) and a coupled peak in the UV-Vis spectrum implying CO-NH
2
interaction between swertiamarin and functionalised GO. The SEM image revealed a sheet-like appearance with an average particle size of 252.38 ± 86.09 nm. The nanoformulation was non-haemolytic at 200 μg/mL (<5%) whereas swertiamarin was haemolytic at 50 μg/mL concentration. The freeze-dried samples exhibited good stability at normal storage condition. The formulation and the swertiamarin displayed similar anticancer activity against HepG2 cell lines with an average IC
50
value of 110 ± 0.75 μg/mL, respectively. Hence, the functionalised GO can be considered as a compatible carrier for bioactive compounds which provides better hemocompatibility and stability. |
Author | K, Sathish Kumar P K, Gayathri |
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CitedBy_id | crossref_primary_10_1016_j_heliyon_2022_e10665 crossref_primary_10_1039_D3BM01391J |
Cites_doi | 10.1021/am5031598 10.1016/S2221-1691(13)60028-3 10.35652/IGJPS.2018.0108 10.1039/C4TX00138A 10.1007/s11706-019-0452-5 10.5772/intechopen.69386 10.4103/0250-474X.34560 10.23937/2378-3664/1410020 10.1016/j.bioorg.2019.103428 10.1002/cber.18980310237 10.1371/journal.pone.0152074 10.3389/fphy.2018.00149 10.1021/nn300172t 10.1186/1743-8977-10-27 10.1007/s11418-016-1026-9 10.1093/toxsci/kfy235 10.1520/F0756-17 10.1021/ja01539a017 10.4236/ojcm.2019.92012 10.1038/srep25518 10.1166/jnn.2018.14296 10.1155/2014/939378 10.1039/C7PY01603D |
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References | cit0011 cit0012 cit0010 Dhande SR (cit0013) 2014; 3 Izawa K (cit0025) 2010; 4 Minghzu Y (cit0018) 2019; 14 cit0019 Mishra N (cit0007) 2017; 5 cit0017 cit0015 cit0016 cit0014 cit0022 cit0001 cit0023 cit0020 cit0021 cit0008 cit0006 cit0028 cit0029 cit0004 cit0026 cit0005 Alam P (cit0009) 2009; 1 cit0027 cit0002 cit0024 cit0003 |
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Snippet | This study aimed to enhance the stability and compatibility of swertiamarin by loading it on amino-functionalised graphene oxide (GO) by ultrasonication. The... |
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SubjectTerms | Functionalised nanocarrier good Stability hemocompatibility hepg2 cell lines nanoformulation sem analysis swertiamarin |
Title | Functionalised nanoformulation of Swertiamarin with enhanced stability and hemocompatibility: synthesis, characterisation and anticancer evaluation |
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