Method of inhibiting restenosis using bisphosphonates

a technology of bisphosphonates and restenosis, which is applied in the direction of phosphorous compound active ingredients, inorganic non-active ingredients, drug compositions, etc., can solve the problems of precisely the problem, the patient is placed at risk of a variety of complications, and the proportion of restenosis is substantial, so as to achieve the effect of treating or preventing restenosis and preventing restenosis

Inactive Publication Date: 2007-07-19
GOLOMB GERSHON +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0009] In a further embodiment, the present invention includes a method of treating or preventing restenosis by administering to an individual, an effective amount of any compound or composite known to inactivate or inhibit blood monocytes and tissue macrophages, thereby treating or preventing restenosis.

Problems solved by technology

However, revascularization induces thrombosis, and neointimal hyperplasia, which in turn cause restenosis in a substantial proportion of coronary arteries after successful balloon angioplasty and in aortacoronary saphenous vein bypass graft and other coronary grafts.
As a result, the patient is placed at risk of a variety of complications, including heart attack or other ischemic disease, pulmonary embolism, and stroke.
Thus, such procedures can entail the risk of precisely the problems that its use was intended to ameliorate.
The introduction of endovascular stents has reduced the incidence of restenosis, but this problem still remains significant, since restenosis or “over exuberant” tissue healing may occur at the site of stent placement.
Furthermore, being highly hydrophilic and negatively charged, BPs in their free form are almost incapable of crossing cellular membranes.

Method used

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  • Method of inhibiting restenosis using bisphosphonates
  • Method of inhibiting restenosis using bisphosphonates
  • Method of inhibiting restenosis using bisphosphonates

Examples

Experimental program
Comparison scheme
Effect test

example 1

Liposomes of Clodronate

[0063] Stock solutions of clodronate were prepared by dissolving the drug in deionized water at a concentration of 0.11 M, pH=7.

Liposome Preparation

[0064] 38.9 mg of distearoylphosphatidylglycerol (DSPG), 118.5 mg of distearoyl-phosphatidylcholine (DSPC) and 38.7 mg of cholesterol were accurately weighed and dissolved in 20 ml of chloroform: methanol (9:1) in a round bottom vial. The vial was gently warmed, and the solvent was then evaporated in rotavapor. 20 mls of hydrated diisopropylether were then added and the vial was put into a water bath until the contents were dissolved. 8 mls of the clodronate solution prepared as described above were then added, and the solution was sonicated at 55° C. for a period of 45 minutes. The organic phase was then evaporated in rotavapor (55° C., 100 rpm). Similarly, other drug-containing liposomes can be prepared.

Purification of Prepared Liposomes

[0065] A Sephadex gel was prepared by dissolving 2.6 grams of Sephade...

example 2

[0074] The antirestenotic effects of liposomal clodronate injections were studied in the balloon-injured rat and hypercholesterolemic rabbit carotid arterial models. The rats were treated by clodronate-containing liposomes, empty liposomes (control), and clodronate in solution (additional control). The dose of clodronate injected was 1.5 and 15 mg / kg administered one day before procedure (−1) and / or on day 6 (+6) post injury. The rabbits (following 30 days of atherosclerotic diet) were treated one day prior to balloon angioplasty by liposomal clodronate (10 mg / kg). The lumen, neointimal, medial and vessel areas and volumes were measured in the treated and control animal groups by digital planimetry of histological sections, at 14 and 30 days post injury in the rat and rabbit models, respectively.

[0075] The results of the antirestenotic effects of liposomal clodronate are shown in FIG. 4. As illustrated, no significant differences were found between treatments with empty liposomes, ...

example 3

Effect of Liposomal Clodronate on IL-1β Production and Transcription and MMP-2 Activity

[0078] The effects of liposomal clodronate on interleukin 1-β (IL-1β) production and transcription and matrix metalloproteinase-2 (MMP-2) activity were studied in the balloon-injured rat and the hypercholesterolemic rabbit carotid arterial models. A group of male Sabra Rats was prepared according to the rat carotid catheter injury model described supra, in Example 1. The hypercholesterolemic rabbit model consisted of New Zealand White rabbits weighing 2.5-3.5 kg. The rabbits were fed an atherogenic diet of 2% cholesterol and 6% peanut oil starting 30 days before angioplasty and hypercholesterolemia was established (plasma cholesterol>1,200 mg / dL). The rabbits were then anesthesized by xylazine (7 mg / kg) and ketamine (40 mg / kg). Heparin (200 units / kg), atropine (0.05 mg) and norfloxacin nicotinate (70 mg) were also administered to the rabbits. Thereafter, balloon injury was performed on the left c...

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Abstract

A method of inhibiting the activity or production of cytokines or growth factors associated with vascular restenosis, by administering to an individual an effective amount of an active ingredient comprising a bisphosphonate particle or a bisphosphonate particulate. The bisphosphonate may be encapsulated, embedded or adsorbed within the particle, dispersed uniformly in the polymer matrix, adsorbed on the particle surface, or in combination of any of these forms. The particles include liposomes or inert polymeric particles, such as microcapsules, nanocapsules, nanoparticles, nanospheres, or microparticles. The particulates include any suspended or dispersed form of the bisphosphonate which is not encapsulated, entrapped, or adsorbed within a polymeric particle. The particulates include suspended or dispersed colloids, aggregates, flocculates, insoluble salts and insoluble complexes of the active ingredient. The cytokines and growth factors include, but are not limited to interleukin 1-β, matrix metalloproteinase-2, and platelet-derived growth factor β (PDGFβ).

Description

[0001] This application is a continuation of application Ser. No. 10 / 160,207 filed on May 30, 2002, which is a continuation-in-part of application Ser. No. 10 / 126,248 filed on Apr. 19, 2002, which is a continuation-in-part of application Ser. No. 09 / 743,705 filed on Mar. 22, 2001, which is a 35 U.S.C §371 filing of PCT application No. PCT / IL99 / 00387 filed on Jul. 14, 1999, which is a continuation-in-part of Israeli application no. 125336 filed on Jul. 14, 1998.FIELD OF THE INVENTION [0002] The present invention is concerned with compositions capable of preventing, inhibiting or reducing restenosis (sometimes referred to in the art as “accelerated arteriosclerosis” and “post-angioplasty narrowing”). Specifically, the invention relates to the use of bisphosphonates (“BP”) to inhibit and / or prevent restenosis. BACKGROUND OF THE INVENTION [0003] Over the past decade, mechanical means of achieving revascularization of obstructive atherosclerotic vessels have been greatly improved. Percut...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): A61K31/675A61K31/66A61K9/14A61K9/00A61K9/10A61K9/127A61K9/51A61K31/00A61K31/663A61K33/242A61K45/00A61K47/02
CPCA61K9/127A61K9/5153A61K31/00A61K31/66Y10S514/824A61K31/675A61K33/24Y10S514/951A61K31/663A61P9/10A61K33/242
Inventor GOLOMB, GERSHONDANENBERG, HAIM
Owner GOLOMB GERSHON
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