Cell adhesion solution

Synthetic resins or natural rubbers -- part of the class 520 ser – Synthetic resins – At least one aryl ring which is part of a fused or bridged...

Reexamination Certificate

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

C523S105000, C524S608000, C435S180000, C528S493000

Reexamination Certificate

active

06657003

ABSTRACT:

FIELD OF THE INVENTION
This invention relates to a liquid solution for coating substrates that demonstrates long-term stability cell adhesion properties and, more particularly, to a solution including a cross-linked amino acid polymer for applying to cytological specimen slides.
BACKGROUND OF THE INVENTION
Many diagnostic assays depend on the evaluation of cytological and histological components. One requirement of these evaluations is the adhesion of these components to a solid substrate, such as a glass or plastic microscope slide. Once immobilized by adhesion, these components may be processed further to gain diagnostic information.
Several cytological/histological adhesion reagents have been developed and used in the past, such as albumin, silane, gelatin, and poly l-lysine. Although all are effective adhesive reagents to some degree, their adhesive properties do not remain stable once coated, applied, and dried on a solid substrate. This results in the need to prepare freshly coated slides for optimal routine use.
SUMMARY OF THE INVENTION
The present invention provides a solution of a cross-linked polymer for substrates. The solution includes an amino acid polymer, a buffered cross-linking agent, and deionized water (DI H
2
O).
In one embodiment, the amino acid polymer, as employed in the invention, is selected from a neutral or basic amino acid, such as but not limited to poly l-lysine or poly 1-arginine.
In another embodiment, the amino acid polymer, as employed in the invention, comprises poly l-lsine.
In another embodiment, the amino acid polymer, as employed in the invention, comprises poly l-lsine of molecular weight of 100,000 or higher.
In another embodiment, the cross-linking agent, as employed in the invention, comprises an aldehyde functional group.
In another embodiment, the cross-linking agent, as employed in the invention, comprises a buffered formaldehyde solution.
In one aspect, the present invention provides a cytological/histological adhesion reagent that retains its adhesive properties in a stable fashion when applied to a solid substrate such as a microscope slide.
In another aspect of the invention, it has been found that poly l-lysine is a suitable cytological adhesion reagent when applied and dried on a glass slide, but that its adhesive properties degraded fairly quickly over time. Poly l-lysine is a three dimensional helical polymeric molecule with side chains containing amine functional groups which effect its adhesive properties. With respect to one aspect of the invention, it was postulated that the physical degradation of this three-dimensional helical structure effectively negated the adhesive abilities of these side chain functional groups. In an attempt to retain this adhesive property of the poly l-lysine coated slides, the concept of stabilizing the poly l-lysine molecule structure was considered a viable solution.
In another aspect of the invention, a stabilization process is provided to cross-link the poly l-lysine molecule using formaldehyde. It is believed that the formaldehyde molecules link the functional groups on the end of the side chains back into the molecular framework, thus physically stabilizing the three-dimensional structure.


REFERENCES:
patent: 4894339 (1990-01-01), Hanazato et al.
patent: 5244787 (1993-09-01), Key et al.
patent: 5505952 (1996-04-01), Jiang
patent: 0856539 (1998-05-01), None
patent: 08296177 (1996-12-01), None
West, Latour and Hench, “Molecular modeling study of adsorption of poly-L-lysine onto silica glass,” CCC 0021-0304/97/040585-07, 1997, John Wiley & Sons Inc.
Chen X et al: “Universal isolation of cross-linked peptides: application to neurofibrillary tangles.” Bioconjugate Chemistry. United States Jan.-Feb. 1999, vol. 10, No. 1, pp. 112-118, XPOO2216566 ISSN: 1043-1802.
Mege J L et al: “Use of cell contour analysis to evaluate the affinity between macrophages and glutaraldehyde-treated erythrocytes.” Biophysical Journal. United States Aug. 1987, vol. 52, No. 2, pp. 117-186, XPOO2216567 ISSN: 006-3495.
Volkov V S et al: “Interaction of Monomeric Components of Nucleic-Acids with Histone and Poly Lysine in Presence of Formaldehyde” Biochemistry (English Translation of Biokhimiya), vol. 46. No. 10 Part 2, 1981, pp. 1448-1453, XPOO1106229 ISSN: 0006-2979.
Winblade N D et al: “Blocking adhesion to cell and tissue surfaces by the chemisorption of a poly-L-lysine-graft-(poly(ethylene glycol); phenylboronic acid) copolymer.” Biomacromolecules. United States 2000 Winter,.
Mcconachie A et al: “The effect on bioadhesive polymers either freely in solution or covalently attached to a support on human macrophages.” Biomedical Sciences Instrumentation. United States 1999, vol. 35, 1999, pp. 45-50, XPOO2216569 ISSN: 0067-8856.
Melius P: “Structure of Thermal Polymers of Amino-Acids” Biosystems, vol. 15, No. 4, 1982, pp. 275-280, XPOO2216570 ISSN: 0303-2647.
Watts et al., “The Use of Cationic Polyelectrolytes in the Preparation of Cell Monolayers for AutomatedCell Scanning and Diagnostic Cytopathology,” 272-278, Analytical and Quantitative Cytology (1984).
Chapter IV, The Chemistry of Fixation, Reference book, poblisher and date unknown.

LandOfFree

Say what you really think

Search LandOfFree.com for the USA inventors and patents. Rate them and share your experience with other people.

Rating

Cell adhesion solution does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with Cell adhesion solution, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Cell adhesion solution will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFUS-PAI-O-3133801

  Search
All data on this website is collected from public sources. Our data reflects the most accurate information available at the time of publication.