• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Selective targeting of magnetic albumin microspheres to the Yoshida sarcoma: ultrastructural evaluation of microsphere disposition.

作者信息

Widder K J, Marino P A, Morris R M, Howard D P, Poore G A, Senyei A E

出版信息

Eur J Cancer Clin Oncol. 1983 Jan;19(1):141-7. doi: 10.1016/0277-5379(83)90409-1.

DOI:10.1016/0277-5379(83)90409-1
PMID:6682772
Abstract

Magnetic albumin microspheres (1 micron average diameter) were selectively targeted to subcutaneous solid Yoshida sarcoma tumors (average size 450 mm2) in Holtzman rats. This was accomplished by placing an external magnet adjacent to the tumor while the microspheres were infused. Microspheres contained ultra-fine particles of Fe3O4 and no drug (placebo). Placebo microspheres were used due to the previously demonstrated rapid tumoricidal effect of targeted low-dose doxorubicin microspheres. Animals were killed 10 min, 60 min, 30 min, 24 hr and 72 hr after microsphere administration and tumors were examined by transmission electron microscopy to determine the in vivo disposition of the magnetically targeted microspheres. Using placebo microspheres, we have demonstrated microspheres endocytosed in endothelial cells as early as 10 min after infusion. By 30 min microspheres can be seen in the extravascular compartment, sitting adjacent to tumor cells and occasionally in tumor cells. By 24 hr the majority of microspheres have been endocytosed by tumor cells. Microspheres were still observed within tumor cells as late as 72 hr after administration. The rapid extravasation and cellular uptake of magnetically focused microspheres explains the extremely rapid tumoricidal effect previously observed when doxorubicin-containing microspheres were targeted to the tumor.

摘要

相似文献

1
Selective targeting of magnetic albumin microspheres to the Yoshida sarcoma: ultrastructural evaluation of microsphere disposition.
Eur J Cancer Clin Oncol. 1983 Jan;19(1):141-7. doi: 10.1016/0277-5379(83)90409-1.
2
Selective targeting of magnetic albumin microspheres containing low-dose doxorubicin: total remission in Yoshida sarcoma-bearing rats.
Eur J Cancer Clin Oncol. 1983 Jan;19(1):135-9. doi: 10.1016/0277-5379(83)90408-x.
3
Tumor remission in Yoshida sarcoma-bearing rts by selective targeting of magnetic albumin microspheres containing doxorubicin.通过选择性靶向含阿霉素的磁性白蛋白微球实现吉田肉瘤荷瘤大鼠的肿瘤缓解。
Proc Natl Acad Sci U S A. 1981 Jan;78(1):579-81. doi: 10.1073/pnas.78.1.579.
4
Treatment of a syngeneic rat tumor with magnetically responsive albumin microspheres labeled with doxorubicin or protein A.用阿霉素或蛋白A标记的磁响应白蛋白微球治疗同基因大鼠肿瘤。
Gynecol Oncol. 1987 May;27(1):34-43. doi: 10.1016/0090-8258(87)90228-9.
5
Targeted delivery of low dose doxorubicin hydrochloride administered via magnetic albumin microspheres in rats.通过磁性白蛋白微球向大鼠靶向递送低剂量盐酸多柔比星
J Microencapsul. 1990 Jan-Mar;7(1):85-94. doi: 10.3109/02652049009028426.
6
Magnetic targeting of microspheres in blood flow.
Microvasc Res. 1984 May;27(3):353-69. doi: 10.1016/0026-2862(84)90065-7.
7
Ultrastructural disposition of adriamycin-associated magnetic albumin microspheres in rats.
J Pharm Sci. 1989 Apr;78(4):290-4. doi: 10.1002/jps.2600780406.
8
Drug targeting: magnetically responsive albumin microspheres--a review of the system to date.
Gynecol Oncol. 1981 Aug;12(1):1-13. doi: 10.1016/0090-8258(81)90089-5.
9
Effect of carrier dose on the multiple tissue disposition of doxorubicin hydrochloride administered via magnetic albumin microspheres in rats.
J Pharm Sci. 1989 Sep;78(9):745-8. doi: 10.1002/jps.2600780909.
10
Comparative disposition of adriamycin delivered via magnetic albumin microspheres in presence and absence of magnetic field in rats.
Life Sci. 1990;46(7):471-9. doi: 10.1016/0024-3205(90)90002-9.

引用本文的文献

1
Development of high-efficiency superparamagnetic drug delivery system with MPI imaging capability.具有磁共振成像能力的高效超顺磁性药物递送系统的研发。
Front Bioeng Biotechnol. 2024 Mar 20;12:1382085. doi: 10.3389/fbioe.2024.1382085. eCollection 2024.
2
Recent advances in nanomaterial-based drug delivery systems for melanoma therapy.用于黑色素瘤治疗的基于纳米材料的药物递送系统的最新进展。
ADMET DMPK. 2023 Oct 24;12(1):107-150. doi: 10.5599/admet.2088. eCollection 2024.
3
Evolution and Clinical Translation of Drug Delivery Nanomaterials.
药物递送纳米材料的进化与临床转化
Nano Today. 2017 Aug;15:91-106. doi: 10.1016/j.nantod.2017.06.008. Epub 2017 Aug 2.
4
Iron oxide nanoparticles for magnetically-guided and magnetically-responsive drug delivery.用于磁导向和磁响应药物递送的氧化铁纳米颗粒。
Int J Mol Sci. 2015 Apr 10;16(4):8070-101. doi: 10.3390/ijms16048070.
5
Development and characterization of nanoparticles for the delivery of gemcitabine hydrochloride.用于盐酸吉西他滨递送的纳米颗粒的研发与表征
ScientificWorldJournal. 2014 Jan 27;2014:560962. doi: 10.1155/2014/560962. eCollection 2014.
6
Gemcitabine-loaded albumin nanospheres (GEM-ANPs) inhibit PANC-1 cells in vitro and in vivo.载吉西他滨白蛋白纳米球(GEM-ANPs)在体外和体内抑制 PANC-1 细胞。
Nanoscale Res Lett. 2013 Apr 17;8(1):176. doi: 10.1186/1556-276X-8-176.
7
Manipulation of magnetic nanoparticle retention and hemodynamic consequences in microcirculation: assessment by laser speckle imaging.利用激光散斑成像评估在微循环中对磁性纳米颗粒滞留和血液动力学后果的操控。
Int J Nanomedicine. 2012;7:2817-27. doi: 10.2147/IJN.S31730. Epub 2012 Jun 11.
8
Preparation of albumin nanospheres loaded with gemcitabine and their cytotoxicity against BXPC-3 cells in vitro.载吉西他滨白蛋白纳米球的制备及其对BXPC-3细胞的体外细胞毒性
Acta Pharmacol Sin. 2009 Sep;30(9):1337-43. doi: 10.1038/aps.2009.125.
9
Magnetic nanoparticle drug carriers and their study by quadrupole magnetic field-flow fractionation.磁性纳米颗粒药物载体及其通过四极磁场流分馏法的研究。
Mol Pharm. 2009 Sep-Oct;6(5):1290-306. doi: 10.1021/mp900018v.
10
Surface modified superparamagnetic iron oxide nanoparticles: as a new carrier for bio-magnetically targeted therapy.表面改性超顺磁性氧化铁纳米粒子:作为生物磁靶向治疗的新型载体
J Mater Sci Mater Med. 2007 Dec;18(12):2297-302. doi: 10.1007/s10856-007-3130-6. Epub 2007 Jun 12.