Francisco Silva, Carolina Mendes, Alice D'Onofrio, Maria Paula Cabral Campello, Fernanda Marques, Teresa Pinheiro, Kyle Gonçalves, Sérgio Figueiredo, Lurdes Gano, Mauro Ravera, Elisabetta Gabano, António Paulo
{"title":"图像引导纳米递送Pt(IV)前药至grp受体阳性肿瘤。","authors":"Francisco Silva, Carolina Mendes, Alice D'Onofrio, Maria Paula Cabral Campello, Fernanda Marques, Teresa Pinheiro, Kyle Gonçalves, Sérgio Figueiredo, Lurdes Gano, Mauro Ravera, Elisabetta Gabano, António Paulo","doi":"10.7150/ntno.78807","DOIUrl":null,"url":null,"abstract":"<p><p>Over the last decades, gold nanoparticles (AuNPs) have proven to be remarkable tools for drug delivery and theranostic applications in cancer treatment. On the other hand, Pt(IV) prodrugs have been employed as an interesting alternative to the more common Pt(II) complexes, such as cisplatin, for cancer chemotherapy. Searching to design an image-guided nanocarrier to deliver selectively Pt(IV) prodrugs to tumors expressing the gastrin releasing peptide receptor (GRPR), we have synthesized small core AuNPs carrying a thiolated DOTA derivative, a GRPR-targeting bombesin analog (BBN[7-14]) and a Pt(IV) prodrug attached to the AuNPs without (<b>AuNP-BBN-Pt1</b>) or with a PEGylated linker (<b>AuNP-BBN-Pt2</b> and <b>AuNP-BBN-Pt3</b>). In the GRPR+ prostate cancer PC3 cell line, the cytotoxic activity of the designed <b>AuNP-BBN-Pt</b> nanoparticles is strongly influenced by the presence of the PEGylated linker. Thus, <b>AuNP-BBN-Pt1</b> displayed the lowest IC<sub>50</sub> value (9.3 ± 2.3 µM of Pt), which is comparable to that exhibited by cisplatin in the same cell line. In contrast, <b>AuNP-BBN-Pt1</b> showed an IC<sub>50</sub> value of 97 ± 18 µM of Pt in the non-tumoral RWPE-1 prostate cells with a much higher selective index (SI) towards PC3 cells (SI = 10) when compared with cisplatin (SI = 1.3). The AuNPs were also successfully labeled with <sup>67</sup>Ga and the resulting <b><sup>67</sup>Ga-AuNP-BBN-Pt</b> were used to assess their cellular uptake in PC3 cells, with <b>AuNP-BBN-Pt1</b> also displaying the highest cellular internalization. Finally, intratumoral administration of <b><sup>67</sup>Ga-AuNP-BBN-Pt1</b> in a PC3 tumor-bearing mice showed a prolonged retention of the nanoparticle compared to that of cisplatin, with optimal <i>in vivo</i> stability and 20% of the injected platinum remaining in the tumor after 72 h post-injection. Furthermore, microSPECT imaging studies confirmed the uptake and considerable retention of the <sup>67</sup>Ga-labeled AuNPs in the tumors. Overall, these results show the potential of these targeted AuNPs loaded with Pt(IV) prodrugs for prostate cancer theranostics.</p>","PeriodicalId":36934,"journal":{"name":"Nanotheranostics","volume":"7 1","pages":"22-40"},"PeriodicalIF":0.0000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9760368/pdf/","citationCount":"1","resultStr":"{\"title\":\"Image-Guided Nanodelivery of Pt(IV) Prodrugs to GRP-Receptor Positive Tumors.\",\"authors\":\"Francisco Silva, Carolina Mendes, Alice D'Onofrio, Maria Paula Cabral Campello, Fernanda Marques, Teresa Pinheiro, Kyle Gonçalves, Sérgio Figueiredo, Lurdes Gano, Mauro Ravera, Elisabetta Gabano, António Paulo\",\"doi\":\"10.7150/ntno.78807\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Over the last decades, gold nanoparticles (AuNPs) have proven to be remarkable tools for drug delivery and theranostic applications in cancer treatment. On the other hand, Pt(IV) prodrugs have been employed as an interesting alternative to the more common Pt(II) complexes, such as cisplatin, for cancer chemotherapy. Searching to design an image-guided nanocarrier to deliver selectively Pt(IV) prodrugs to tumors expressing the gastrin releasing peptide receptor (GRPR), we have synthesized small core AuNPs carrying a thiolated DOTA derivative, a GRPR-targeting bombesin analog (BBN[7-14]) and a Pt(IV) prodrug attached to the AuNPs without (<b>AuNP-BBN-Pt1</b>) or with a PEGylated linker (<b>AuNP-BBN-Pt2</b> and <b>AuNP-BBN-Pt3</b>). In the GRPR+ prostate cancer PC3 cell line, the cytotoxic activity of the designed <b>AuNP-BBN-Pt</b> nanoparticles is strongly influenced by the presence of the PEGylated linker. Thus, <b>AuNP-BBN-Pt1</b> displayed the lowest IC<sub>50</sub> value (9.3 ± 2.3 µM of Pt), which is comparable to that exhibited by cisplatin in the same cell line. In contrast, <b>AuNP-BBN-Pt1</b> showed an IC<sub>50</sub> value of 97 ± 18 µM of Pt in the non-tumoral RWPE-1 prostate cells with a much higher selective index (SI) towards PC3 cells (SI = 10) when compared with cisplatin (SI = 1.3). The AuNPs were also successfully labeled with <sup>67</sup>Ga and the resulting <b><sup>67</sup>Ga-AuNP-BBN-Pt</b> were used to assess their cellular uptake in PC3 cells, with <b>AuNP-BBN-Pt1</b> also displaying the highest cellular internalization. Finally, intratumoral administration of <b><sup>67</sup>Ga-AuNP-BBN-Pt1</b> in a PC3 tumor-bearing mice showed a prolonged retention of the nanoparticle compared to that of cisplatin, with optimal <i>in vivo</i> stability and 20% of the injected platinum remaining in the tumor after 72 h post-injection. Furthermore, microSPECT imaging studies confirmed the uptake and considerable retention of the <sup>67</sup>Ga-labeled AuNPs in the tumors. Overall, these results show the potential of these targeted AuNPs loaded with Pt(IV) prodrugs for prostate cancer theranostics.</p>\",\"PeriodicalId\":36934,\"journal\":{\"name\":\"Nanotheranostics\",\"volume\":\"7 1\",\"pages\":\"22-40\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9760368/pdf/\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Nanotheranostics\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.7150/ntno.78807\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"Pharmacology, Toxicology and Pharmaceutics\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nanotheranostics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.7150/ntno.78807","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"Pharmacology, Toxicology and Pharmaceutics","Score":null,"Total":0}
Image-Guided Nanodelivery of Pt(IV) Prodrugs to GRP-Receptor Positive Tumors.
Over the last decades, gold nanoparticles (AuNPs) have proven to be remarkable tools for drug delivery and theranostic applications in cancer treatment. On the other hand, Pt(IV) prodrugs have been employed as an interesting alternative to the more common Pt(II) complexes, such as cisplatin, for cancer chemotherapy. Searching to design an image-guided nanocarrier to deliver selectively Pt(IV) prodrugs to tumors expressing the gastrin releasing peptide receptor (GRPR), we have synthesized small core AuNPs carrying a thiolated DOTA derivative, a GRPR-targeting bombesin analog (BBN[7-14]) and a Pt(IV) prodrug attached to the AuNPs without (AuNP-BBN-Pt1) or with a PEGylated linker (AuNP-BBN-Pt2 and AuNP-BBN-Pt3). In the GRPR+ prostate cancer PC3 cell line, the cytotoxic activity of the designed AuNP-BBN-Pt nanoparticles is strongly influenced by the presence of the PEGylated linker. Thus, AuNP-BBN-Pt1 displayed the lowest IC50 value (9.3 ± 2.3 µM of Pt), which is comparable to that exhibited by cisplatin in the same cell line. In contrast, AuNP-BBN-Pt1 showed an IC50 value of 97 ± 18 µM of Pt in the non-tumoral RWPE-1 prostate cells with a much higher selective index (SI) towards PC3 cells (SI = 10) when compared with cisplatin (SI = 1.3). The AuNPs were also successfully labeled with 67Ga and the resulting 67Ga-AuNP-BBN-Pt were used to assess their cellular uptake in PC3 cells, with AuNP-BBN-Pt1 also displaying the highest cellular internalization. Finally, intratumoral administration of 67Ga-AuNP-BBN-Pt1 in a PC3 tumor-bearing mice showed a prolonged retention of the nanoparticle compared to that of cisplatin, with optimal in vivo stability and 20% of the injected platinum remaining in the tumor after 72 h post-injection. Furthermore, microSPECT imaging studies confirmed the uptake and considerable retention of the 67Ga-labeled AuNPs in the tumors. Overall, these results show the potential of these targeted AuNPs loaded with Pt(IV) prodrugs for prostate cancer theranostics.