Injectable cross-linked polymeric preparations and uses thereof

a cross-linked polymer and injection technology, applied in the direction of drugs, cardiovascular disorders, prosthesis, etc., can solve the problems of early ventricular rupture or aneurysm formation, progressive deterioration of contractile function, heart failure and death, etc., to promote the regeneration of damaged myocardium and increase its function.

Inactive Publication Date: 2005-01-06
BEN GURION UNIVERSITY OF THE NEGEV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

As described herein, the present inventors developed a cross-linked alginate biomaterial which flows as liquid but still maintains sufficient consistency until injection into the desired location in the body, where it forms a solid gel. Most surprisingly, injection of this cross-linked alginate biomaterial promotes regeneration of damaged myocardium and increase of its function, without the need of cell co-transplantation. Thus, the use of these injectable polymeric solutions to treat cardiac infarcts may be an efficient replacement for treatments based on embryonic cell transplantation, in the treatment of myocardial infarct (MI) and chronic heart failure (CHF).

Problems solved by technology

The early phase of LV remodeling involves expansion of the infarct zone, which may result in early ventricular rupture or aneurysm formation.
It results in progressive deterioration in contractile function, heart failure and death [Sutton, M. G. and Sharpe, N.
However, current clinical interventions to minimize the devastating effects of heart attack are frequently not sufficient to prevent irreversible damage, LV remodeling and subsequent development of heart failure and death [Khand, A. U. et al.
However, cell transplantation approaches may be of little clinical benefit when the local cardiac structure cannot support cell seeding because it is absent or seriously damaged.
This strategy, however, might be limited due to lack of appropriate cells, risk of surgical procedure, general anesthesia and restricted access to LV septum and inferior wall.
However, the behavior of the system was less than satisfactory.
However, the consistency of hydrogel-cell suspensions of the type described above is not totally satisfactory for the purpose of injection into patients in need.
In particular, the shortcoming of these injectable cell-alginate formulations which disallows its use in clinical trials is the inconsistent performance between lots, due to poor distribution of the components during formulation.
This may be a considerable disadvantage.
These are evident disadvantages in the rather long process of tissue regeneration.

Method used

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  • Injectable cross-linked polymeric preparations and uses thereof
  • Injectable cross-linked polymeric preparations and uses thereof
  • Injectable cross-linked polymeric preparations and uses thereof

Examples

Experimental program
Comparison scheme
Effect test

example 1

Preparation and Rheological Evaluation of Injectable Cross-Linked Alginate Biomaterial

The molecular weight (Mw) of the biopolymer alginate and its polydispersity (PD) (indication of the distribution range of molecular weight) may have an effect on the formation rate and structure of the resultant entanglement network. Thus, alginates Mw and PD using GPC-MALLS (as described in Experimental Procedures) were characterized (Table 1).

TABLE 1Alginate characterizationAlginateMn (g / mol)Mw (g / mol)PD (Mw / Mn)LF 5 / 602.102e+42.752e+41.309 ± 0.0072.113e+42.656e+41.257 ± 0.01 LVG1.469e+51.667e+51.135 ± 0.0161.385e+51.559e+51.126 ± 0.012MVG2.103e+52.596e+51.235 ± 0.0062.055e+52.385e+51.161 ± 0.007

Notes:

(i) The two numbers given for each measure represent two different batches of the material.

(ii) g / mol = Dalton

Rheology

The alginate gels fall under the category of physical gels, wherein physical cross-links are formed that are neither permanent nor as strong as covalent cross-links.

Stead...

example 2

Comparing Therapeutic Effects of Alginate Biomaterial to Cardiac Cell Transplantation in a Rat Model of MI

Seven days after extensive MI, rats were randomized to alginate-based biomaterial injections, embryonic cardiomyocyte (1.5×106) implantation, or medium injection into the myocardial scar. The alginate biomaterial was calcium cross-linked, yet it still flowed under injection conditions, as described above. Echocardiography study was performed before and 1 and 2 months after implantation to assess LV remodeling and function. Hearts were harvested two months after implantation for histological evaluation.

Serial echocardiography studies revealed that the cross-linked alginate-based biomaterial injection enhanced scar thickness, prevented LV dilatation and dysfunction, comparable to cardiac cell transplantation, while control animals developed significant LV dilatation accompanied by progressive deterioration in LV contractility. The results are summarized in Table 3.

TABLE 3Al...

example 3

Animal Model of MI Treated with Calcium Cross-Linked Alginate Biomaterial

Overall, 39 rats were included in the study. Thirteen rats died after the surgical procedure to induce MI. Echocardiographic studies and analysis were performed on 24 rats. Fifteen rats were treated with alginate biomaterial injection and the control group (n=9) received injection of serum free culture medium. Two rats received injection of alginate into normal heart to study its safety and effect on normal myocardium.

Echocardiography Functional Study

Alginate biomaterial injection significantly increased scar thickness (Table 4, p<0.0001). Furthermore, it efficiently attenuated the typical course of LV dilatation complicating extensive anterior MI (FIG. 5, Table 4).

Although there was an increase in LV chamber internal diameters and areas, it was significantly less than that observed in control animals (FIG. 5 and Table 4). The beneficial effect of alginate biomaterial on LV remodeling was translat...

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Abstract

A composition for promoting repair of damaged tissues, being a cross-linked alginate solution, which can be maintained in liquid form indefinitely (under constant conditions) and only gels in vivo. This cross-linked alginate solution is an ideal material to be used for tissue repair. Injection of said material into cardiac tissue post-myocardial infarct induced tissue regeneration. The invention provides such injectable solution, as well as compositions and method of preparation thereof. The invention also provides various methods and uses of the cross-linked alginate solution, for cardiac tissue regeneration, induction of neo-vascularization, enhancing SDF-1 expression and guiding stem cell chemotaxis, among others. A kit for tissue repair is also provided.

Description

FIELD OF THE INVENTION The present invention relates to injectable pharmaceutical preparations containing cross-linked polymer, particularly alginate, as an active ingredient, which polymer forms a hydrogel in vivo. The invention also relates to the various uses of the injectable cross-linked alginate preparations and to methods of treatment employing the same, particularly repair of cardiac tissue damage and ablation of cardiac arrhythmias. BACKGROUND OF THE INVENTION All publications mentioned throughout this application are fully incorporated herein by reference, including all references cited therein. Myocardial infarction (MI) results in acute loss of myocardium and in an abrupt increase in loading conditions that induces left ventricular (LV) remodeling [Sutton, M. G. and Sharpe, N. (2000) Circulation 101:2981-2988; Mann, D. L. (1999) Circulation 100:999-1008; Jugdutt, B. I. (2003) Circulation 108:1395-1403]. The early phase of LV remodeling involves expansion of the infarc...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): A61L27/20A61L27/52
CPCA61K9/0024A61L27/20A61L27/52A61L2400/06A61L2430/20A61K35/33A61K45/06A61K31/738A61K35/12A61K35/34A61K31/734C08L5/04A61P19/04A61P29/00A61P31/00A61P9/00A61P9/06A61P9/10A61L27/00
Inventor COHEN, SMADARLEOR, JONATHAN
Owner BEN GURION UNIVERSITY OF THE NEGEV
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