Nanoparticle Therapeutics 2022
DOI: 10.1016/b978-0-12-820757-4.00012-0
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Radioactive nanoparticles and their biomedical application in nanobrachytherapy

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Cited by 3 publications
(6 citation statements)
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“…56,57 The possible explanation of obtained results can be associated with several factors, including metal ion complexation (known to be strong for L-cysteine, L-histidine, and L-methionine), the metal-binding affinity of amino acids to the metal surface, 55 and structure of intermediate decomposition (Scheme 2), which may or may not facilitate the further formation of AuNPs. 19,20,58−61 The reduction of HAuCl 4 with salts of 11 studied α-amino acids, 1−6, 12, 14, 15, 17, and 18, which constitute α-amino acids with aliphatic (Gly (1), Ala (2), Val (3), Leu (4), and Ile (5)), aromatic (Phe (6)), amidated (Asn ( 12)), hydroxylated (Ser (14) and Thr ( 15)), and acidic (Glu (17) and Asp ( 18)) side chains yielded mono-or polydisperse quasi-spherical AuNPs with sizes ranging from 10 to over 60 nm and different size distributions (Figures 1, 2, S1, and S2; Table 1). Considering the molecular structure of these 11 α-AA (no functional groups on side chains capable of reducing tetrachloroaurate ions) and the results of their reactions with HAuCl 4 , it can be confirmed that the rate-determining step of gold salts reduction with α-AA anions occurs via mechanism proposed in Scheme 2.…”
Section: ■ Results and Discussionmentioning
confidence: 60%
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“…56,57 The possible explanation of obtained results can be associated with several factors, including metal ion complexation (known to be strong for L-cysteine, L-histidine, and L-methionine), the metal-binding affinity of amino acids to the metal surface, 55 and structure of intermediate decomposition (Scheme 2), which may or may not facilitate the further formation of AuNPs. 19,20,58−61 The reduction of HAuCl 4 with salts of 11 studied α-amino acids, 1−6, 12, 14, 15, 17, and 18, which constitute α-amino acids with aliphatic (Gly (1), Ala (2), Val (3), Leu (4), and Ile (5)), aromatic (Phe (6)), amidated (Asn ( 12)), hydroxylated (Ser (14) and Thr ( 15)), and acidic (Glu (17) and Asp ( 18)) side chains yielded mono-or polydisperse quasi-spherical AuNPs with sizes ranging from 10 to over 60 nm and different size distributions (Figures 1, 2, S1, and S2; Table 1). Considering the molecular structure of these 11 α-AA (no functional groups on side chains capable of reducing tetrachloroaurate ions) and the results of their reactions with HAuCl 4 , it can be confirmed that the rate-determining step of gold salts reduction with α-AA anions occurs via mechanism proposed in Scheme 2.…”
Section: ■ Results and Discussionmentioning
confidence: 60%
“…In our studies, we used for the synthesis of AuNPs salts of twenty-one α-amino acids (Chart 1). Among the used reagents were Lglycine (Gly) (1), L-alanine (Ala) (2), L-valine (Val) (3), Lleucine (Leu) (4), L-isoleucine (Ile) (5), DL-phenylalanine (Phe) (6), L-tryptophan (Trp) (7), L-methionine (Met) (8), L-proline (Pro) (9), L-cysteine (Cys) (10), L-glutamine (Gln) (11), L-asparagine (Asn) (12), L-tyrosine (Tyr) (13), L-serine (Ser) (14), DL-threonine (Thr) (15), L-(4)-hydroxyproline (Hyp) (16), L-glutamic acid (Glu) (17), L-aspartic acid (Asp) (18), L-histidine (His) (19), L-lysine (Lys) (20), and Larginine (Arg) (21). All investigated α-amino acids consist of a carboxyl group and an amine group in the α-position to it but differ in the side chain structure, giving each amino acid unique physicochemical properties (Table S2).…”
Section: ■ Results and Discussionmentioning
confidence: 99%
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“…As an alternative to NaBH 4 , we also explored reduction using ascorbic acid, heating, or irradiation with light at neutral pH and, besides Ag or Au NPs, we also prepared AgAu alloy NPs at a molar ratio of 1:1. 101 In all cases, NP synthesis in the presence of the polyampholytic graft copolymer was successful, resulting in stable dispersions of Ag, Au, and AgAu NPs (Figure 5). Although Ag NPs and Au NPs in all cases revealed their characteristic absorbance maxima at 415−420 and 525−550 nm, respectively, in case of the resulting alloys, this was found at 440−490 nm, indicating the formation of an alloy instead of both noble-metal NPs individually, because a physical mixture of both individual NPs would result in a bimodal distribution, as shown in Figure S6.…”
Section: ■ Results and Discussionmentioning
confidence: 93%
“…Frequently, the reason for this is related to insufficient plasmonic signal enhancement generated by commercially available gold nanoparticles (AuNPs). Nanocolloids prepared by single-step approaches like laser ablation (no specificity in NP shape), 15 or more complex methods like thermal-based electrochemical reduction 16 (additional reducing agent involved) are not characterized by sufficient stability or adhesion on the supporting substrate. Analytical difficulties can be attributed to nonhomogeneous NP distribution over the surface, leading to problems with SERS hot-spot populations.…”
mentioning
confidence: 99%