Adduct of fluorescent dye and tumor avid tetrapyrrole

一种荧光染料、染料的技术,应用在荧光染料和肿瘤亲和的四吡咯的加合物领域,能够解决缺少优选肿瘤吸收度、毒性、破坏肿瘤增生性组织等问题

Inactive Publication Date: 2007-06-20
HEALTH RES INC
View PDF16 Cites 2 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, such an approach has notable difficulties due to several factors including: lack of significant preferential tumor uptake, toxicity, and lack of sufficient penetration, whether due to activation of the fluorescent compound or already sufficiently penetrated in the tumor or emissions detected in vitro
Furthermore, such compounds, while potentially detectable, do not function to destroy tumors and other hyperplastic tissues

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Adduct of fluorescent dye and tumor avid tetrapyrrole
  • Adduct of fluorescent dye and tumor avid tetrapyrrole
  • Adduct of fluorescent dye and tumor avid tetrapyrrole

Examples

Experimental program
Comparison scheme
Effect test

specific example

[0047] Specific examples of dyes used in the present invention are as follows: indocyanine green (bisindole, i.e. tricarbocyanine type dye); indocyanine green 820nm analog CAS172616-80-7 (R 7d yes ); Fast Green FCF (FD & C Green 3, a triphenylmethane dye); Supan blue (triphenylmethane dye) and methylene blue (thiazine dye).

[0048] The tumor-affinitive tetrapyrrole compound is preferably a porphyrin derivative (including porphyrin-related compounds, whether actually derived from porphyrin or not), usually selected from chlorins, bacteriochloroins and bacteriohinoids. Preferred porphyrin derivatives generally have the following general structure:

[0049]

[0050] in:

[0051] R 1 is substituted or unsubstituted -CH=CH 2 , -CHO, COOH, or

[0052] where R 9 =-OR 10 , where R 10 is a lower alkyl group of 1 to 8 carbon atoms, or -(CH 2 -O)nCH 3 ; 2 , R 2a , R3 , R 3a , R 4 , R 5 , R 5a , R 7 , and R 7a independently hydrogen, lower alkyl, substituted lowe...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

No PUM Login to view more

Abstract

A compound having preferential localization in tumor tissue relative to normal tissue, a preferential electromagnetic absorption at a wavelength between about 660 and 900 nm, and a fluorescence at a wavelength shifted from the preferential absorption by at least +30 nm and preferably at least +50nm. The compound further preferably destroys tumor tissue in which it is absorbed when exposed to light at its preferential absorption wavelength. In a preferred embodiment of the invention, the compound is a conjugate of a tumor avid tetrapyrrole compound with a fluorescent dye, and more preferably the fluorescent dye is an indocyanine dye such as indocyanine green. The tumor avid tetrapyrrole compound is preferably a porphyrin derivative selected from the group consisting of chlorins, bacteriochlorins, purpurins and derivatives thereof.

Description

Background of the invention [0001] Detection of early neoplastic changes is important from an outcome standpoint because once invasive cancer and cancer metastasis have occurred, treatment becomes difficult. Currently, excisional biopsy followed by histological examination is considered the "gold standard" for diagnosing early neoplastic changes and carcinomas. Occasionally, cytology, that is, analysis of superficial or excretory cells rather than excisional biopsy, is done. These techniques are powerful diagnostic tools because they provide high-resolution spatial and morphological information about the cellular and subcellular structure of tissues. The contrast and specificity of histopathological detection can be improved through the use of staining and processing. However, both of these diagnostic procedures require physical removal of the sample followed by manipulation of the tissue in the laboratory. These procedures are relatively costly because of the shipping and ...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
Patent Type & Authority Applications(China)
IPC IPC(8): C07D487/22
CPCY10S514/912C07D487/22A61K41/0057A61K49/0052A61K49/0032A61K41/0071A61B10/00A61B5/055A61K31/40C07B47/00
Inventor 拉温德拉·K·潘迪陈亦晖威廉·波特艾伦·奥塞罗夫
Owner HEALTH RES INC
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products