GB2223027A

GB2223027A - Periodontium regenerating materials

Info

Publication number: GB2223027A
Application number: GB8918343A
Authority: GB
Inventors: Yoshito Ikada; Shokyu Gen
Original assignee: GC Dental Industiral Corp
Current assignee: GC Corp
Priority date: 1988-08-31
Filing date: 1989-08-11
Publication date: 1990-03-28
Anticipated expiration: 2009-08-11
Also published as: AU3949089A; GB2223027B; BE1002656A5; AU624847B2; JPH0263465A; FR2635685B1; FR2635685A1; SE8902867L; DK426989D0; GB8918343D0; DE3928933C2; JP2709349B2; CA1340354C; SE8902867D0; SE503230C2; CH679836A5; DK426989A; DE3928933A1

Description

1 1 r)r r3027 A24 PERIODONTIUM-REGENERATIVE MATERIALS The present

invention relates to a bi odegradabl e /absorbable dental material required for the regeneration of the tissues of a living body attacked by periodontosis.

In current periodontal treatments of healthy cementum and periodontal ligament attacked by periodontal diseases, hydroxyapatite and calcium phosphate are used as the alveolar bone fillers to be filled in lost periodontal tissues.

However, such treatments are considered to be only effective to prevent periodontal diseases from reaching an advanced stage or recurring to some degrees. In recent years, the Guided Tissue Regeneration Technic developed by Professor S. Nyman et al (University of Gothenburg) from a biological standpoint of view has attracted attention in dental fields. For such epoch-making Guided Tissue Regeneration Technic, it has been reported that certain results are achievable with what is called Goretex membrane which is neither degradable nor absorbable in a living body. See S. Nyman et a!, "The regenerative potential of the periodontal ligament - An experimental study in the monkey", J. Clin. Periodontol, 9:257, 1982.

Since Coretex membrane is neither degradable nor absorbable in a living body, it constitutes an alien substance to the living body and is reactive to the tissues. Therefore we must take off Coretex membrane after first treatment and second operation is thus again needed. From such a standpoint of view, a report of the studies of using biodegradable/absorbable membranes for the Guided Tissue Z 1 - Z Regeneration Technic has been presented. See I. Magnusson et al, Attachment Formation Following Controlled Tissue Regeneration Using Biodegradable Membranes% J. Periodontol, 59, 1-6, January, 1988.

However. since a homopolymer consisting of 100 % polylactic acid is used as the bio-degradable/absorbable membrane, it is impossible to control both dynamic (or mechanical) properties and a rate of hydrolysis simultaneously.

Due to its glass transition temperature higher than a temperature of a body, the homopolymer consisting of 100 polylactic acid gives a physical stimulus to the soft tissues of a -living body with the resulting inducement of inflammation. With the homopolymer, it is difficult to freely vary the rate of hydrolysis.

The present inventors have made intensive and extensive studies to eliminate the weak points of the above homopolymer of polylactic acid, i. e., to improve especially its dynamic (or mechanical) properties, thermal properties, and the rate of hydrolysis. As a consequence, it has been found that a film or sheet of a lactide/Ecaprolactone or a glycolide copolymer is best-suited for the Guided Tissue Regeneration Technic. Thus, the present invention has been accomplished.

The present invention provides a pe.:iodontium-regenerating material which is a bio-degradable/absorbable high-molicular material, and preferably uses a lactide/r-caprolactone- or a glycolide copolymer as the biodegradable /absorbable high-molecular materials applied to the Guided Tissue Regeneration Technic to be effective to prevent periodontal diseases. Such bio-degradablejabsorbable materials may be formed into films or sheets by dissolving the lactide/ c -caprolactone or lac tide /glycol ide copolymers in a solvent such as an organic solvent, e.g., methylene chloride, chloroform, dioxane toluene, benzene, dime thyl formami de, or acetone and subjecting the resulting solutions to 1 1 casting or hot pressing. In order to allow such films or sheets to transmit body fluids such as nourishment therethrough or give flexibility thereto, they may be made porous by stretching or freezedrying treatment in benzene or dioxane solution.

The bio-degradable/absorbable high-molecular materials according to the present invention excel in not only flexibility but also biocompatibility. Thus, they tend to disappear immediately after a cure of injured sites with no fear of interfering with the bony ankylosis of the connective tissue separated from a surface of a root by discission or lesion. The reason why such excellent biocompatibility is obtained is that it is possible to use materials whose dynamic and thermal properties as well as the rate of hydrolysis can be varied by the copolymerization of lactide that is an aliphatic polyester with e-caprolactone or glycolide used in suitable ratios and that the materials can be selected in application depending upon how much the injured sites are to be cured.

The present invention will now be explained in more detail with reference to the accompanying drawings, which are given for the purpose of illustration alone and in which: - Figure 1 is a graph. showing the relation between the molar fraction of e-caprolactone in the copolymer of L- lactide/ecaprolactone and the glass transition temperature of that copolymer; Figure 2 is a graph illustrating the relation between the molar fraction of --caprolactone in the copolymer of L-lactide/e - caprolactone and the dynamic modulus of elasticity thereof at room temperature; Figure 3 is a graph showing the relation between the time of hydrolysis and the weight and rate of residual molecular weight of the copolymer of L-lactide/F,-caprolactone; and A Figure 4 is a graph. showing the relation between the time of hydrolysis and the tensile strength of the copolymer of Llactide/e -caprolactone.

The bio-degradable /absorbable high-molecular materials used in the present invention are widely distributed in the natural world and are a copolymer of lactide/r;-caprolactone or lac tide /glycol ide found in the bodies of animals. The composition and molecular weight of such a copolymer may be selected depending upon the mechanical properties and bio-degradinglabsorbing rate of material suitable for the condition of a periodontal disease. The lac tide/ c caprolac tone copolymers used in the present invention are synthesized according to the following scheme.

L - lactide monorner Tm.960C D,L - lactide monaner Tm.1280C DIL - lactide, L-lactide CH, 1 OH-C-COOH 1 H CH, 1 -41 O-C-C 1 11 H - 3HC 0 HC _+ 1 O=C C=0 1 CH C H, n 0 ú -caprolactene :2 H C - (C HA.

1 1 U-(-;=U , - caprolactcne mancmer Tm. -50C Ring opening polymerization 3 lic 0 HC C-0 1 1 + U-G CH 0 c H, lactide-caprolactcne ccpolymer 2 H C -(C II, 1 1 U-(J=U CH3 0 1 11 O-CH - 1901C 1 Shours C H, 0 k 1 The copolymers of lactide/glycolidc- used in the T)resent inventinn are synthesized according to the following schmme.

3fIC 0 H C C=O I. I O=C C H \ 0 / \ C H, lactide 0 H2 G=0 + 1 1 O=C UM, 0 Glycolide fl 0-(CH2)3-0 11 U CH, 0 O-CH-0-( CH, U 0 11 O-CH2-0-C-CH.,-C11 U lactictelglicolide copolymer 0 v n 1 1 1 1 The bio-degradable /absorbable high-molecular materials used in the present invention come in touch with the soft tissues of a living body, and axe thus required to have some flexibility, since inflammatory reactions are induced by physical stimuli at the time when there is a large difference between dynamic properties of such materials and those of the soft tissues of a living body, especially, when their hardness is in excess. In order to accomplish this aim, it is preferred that their glass transition temperature is in the vicinity o! a temperature of a body. To meet such a requirement, it is required to select the composition of the lac tide/ r; -caprolac tone or the lactide/glycolide copolymers according to suitable compositional ratios. Figure I illustrates a change in the glass transition temperature on the molar fraction of e-caprolactone in the copolymer of lactide / e -caprolac tone. It is understood that the measurement of glass transition temperature was carried out with a differential scanning calorimeter (DSC) - marked by & and a dynamic modulus meter - marked by 0.

The bio-degradable /absorbable high-molecular materials used in the present invention are required to have a certain dynamic strength. In other words, when there is a need of fixing the biodegradable /absorbable films or sheets to a given region with a suture, a grave problem will arise if the fixed part tears up. In the absence of a certain strength or modulus of elasticity, on the other hand, it poses a problem in connection with the retainment of shape tending to change due to hydrolysis, so that the desired object cannot be attained. Therefore, the materials used in the present invention should preferably have a dynamic modulus in a range of 5 x 101 to 5 X 10s dynes/cm' that is attainable by the selection of the composition of the copolymers. Figure 2 illustrates a change at room temperature in the dynamic modulus of elasticity on the molar fraction P of r--caprolactone in the copolymer of L-lactide/s -caprolactone. lt is understood that the dynamic modulus of elasticity was measured with RheoVibron available from Toyo Balldwin.

On the one hand, the bio-degradable /absorbable high-molecular materials used in the present invention should be retained in the form of a film or a sheet within a period during which the regeneration of the alveolar bone and the recombination of the surface of a root with the connective tissue are achieved. On the other hand, it is not desirable that they remain as an alien substance in a living body after curing. Thus, they are required to be rapidly degraded, absorbed and disappeared. The degradable /absorbable rate can also be controlled by varying a composition and a molecular weight of the copolymers.

Changes in the in-vitro hydrolysis on the molar fraction of e caprolactone in the copolymer of L-lactide/,- -caprolactone therein are illustrated in Figures 3 and 4, wherein 0 stands for 100 % L-lactide molecular weight, D 88 % L-lactide molecular weight, A 65 % Llactide molecular weight, @ 15 % Llactide molecular weight, x 100 % a - caprolactone molecular weight, & 100 % L-lactide mass, a 88 % L-lactide mass, and A 65 01. L-lactide mass. The rate of hydrolysis of samples in the in-vitro were estimated in a solution having a certain volume (3 mm long x 5 mm wide x 1 mm thick) in a phosphate buffer solution of 37 'C (pH 7.4) with an elution tester according to THE PHARMACOPOEIA OF JAPAN. The weight, molecular mass and the rate of reductions of tensile strength of the hydrolysated products were measured before and after hydrolysis and expressed in terms of percentage.

Then, the bi o-degradable /absorbable rates and reactivity to a tissue were investigated by in-vivo tests. The dorsal muscles of house rabbits, each weighing about 3 kg, were incised along the fibrous direction, the samples were filled, and the fasciae were then sutured. Prior to the filling, the samples were sterilized with an ethylene oxide gas. After the filling, the rabbits were slaughtered with the lapse of time to examine changes in the physical properties of the samples and the reactivity of the peripheral tissues. As a consequence, the homopolymer consisting of 100 % polylactic acid remained substantially in its entirety even after the lapse of six months and the soft tissue in touch with the periphery of the material suffered from some inflammation. However, the copolymers of lactide/is caprolac tone (at a molar ratio of 70:30 mol %) and lactide /glycol i de (at a molar ratio of 75:25 mol %) were completely degraded and absorbed with no sign of any tissular reaction.

From the above results, it is appreciated that the copolymers of lac tide/ E, -caprol actone and lactide /glycol ide are superior to the homopolymer consisting of 100 % polylactic acid in the dynamic properties and the rate of hydrolysis as well as the biocompatibility. The copolymers of lacti de / c -caprolac tone and lactide/glycolide are interesting materials since, as is the case with the homopolymer consisting of 100 % polylactic acid, they cause non-enzymatical hydrolysis in a living body to give hydrolyzates which are degraded and absorbed and finally discharged from the living body in the form of water and carbon dioxide. Thus, the bio-degradable/absorbable highmolecular materials according to the present invention are not only useful materials for the Guided Tissue Regeneration Technic, but are also clinically useful materials in other dental fields.

The biodegradable/absorbable high-molecular materials of the present invention will now be explained specifically but not exclusively with reference to the following examples.

Example 1

A fully developed mongrel was forcedly made to suffer from a k 1 periodontal disease, thereby inducing gingival retraction. The biodegradable /absorbable porous film was used in the form of an about 200pm thick sheet consisting of a L-lac tide/ E -caprolactone copolymer (at a molar ratio of 70:30 mol %) having a weight-average molecular weight of about 220,000 as well as a dynamic modulus of elasticity of 9.5 x 107 dynes /CM2 and anelongation rate of 150 Z, both at room temperature (25 'C) - Af ter the surface of the root had been covered with such the sheet in a form of a patched tent, a flap of the gingival tissue was backsutured to prevent the connective tissue from coming in contact with the surface of the root and taking part in the process of healing. After the lapse of three months, the process of healing was observed. As a result, the L-lac tide/ F_ -caprolactone copolymer was found to lose a substantial part of its dynamic strength and cause considerable hydrolysis, although its shape was remained. However, new attachment including a formation of the new alveolar bone indicated that the periodontal disease was cured.

Example 2

As the bio-degradable/absorbable film, use was made of an about 180pm thick film-like material consisting of a D, L-lactide /glycol ide copolymer (at a molar ratio of 80:20 mol Z) having a weight-average molecular weight of 170,000 as well as a dynamip modulus of elasticity 9. 8 x 10 dynes/cml and anelongation rate of 200 Z, both at room temperature (25 'C). According to the procedures of Example 1, the process of healing was estimated after the lapse of three months. As a consequence, it was found that the film consisting of the D,Llactide/glycolide copolymer was substantially degraded and absorbed, and that the periodontal ligament fibers were formed simultaneously with the formation of a new bone, a sign of healing of the periodontal disease.

1 Example 3

A 10 % dioxane solution of a L-lactide/glycolide copolymer (at a molar ratio of 90:10 mol %) having a weight-average molecular weight of about 260,000 as well as a dynamic modulus of elasticity of 1.8 x 108 dynes/cm2 and aK elongation rate of 1000 both at room temperature (25 "C) was freeze-dried to prepare a biodegradable/absorbable porous film in the form of an about 220pm sheet.

With this film, an animal experiment was performed in a similair manner as described in Example 1. After the lapse of three months, it was found that the porous sheet-like film consisting of the L lactide/glycolide copolymer was completely degraded and absorbed with a healing of periodontal disease.

Example 4

A 10 % dioxane solution of a D,L-lactide/glycolide copolymer (at a molar ratio of 75:25 mol %) having a weight-average molecular weight of about 190,000 as well as a dynamic modulus of elasticity of 3.2 x 108 dynes/cm' and an elongation rate of 1500 %, both at room temperature (25 C) was freeze-dried to prepare a biodegradable/absorbable porous film in the form of an about 160pm sheet. With this film, an animal experiment was performed in a similar manner as described in Example 1. After the lapse of three months, it was found that the porous sheet-like film consisting of the D,Llactide/glycolide copolymer was completely degraded and absorbed with a healing of periodontal disease.

Comparative Example 1 An experiment was performed according to Example 1, provided that an about 200pm thick material consisting of polylactic acid having a molecular weight of about 220,000 was used as the biodegradable/absorbable film, to observe the degree of healing after the lapse of three months. As a result, it was found that the polylactic i; 1 acid film was not substantially degraded with the inducement of partial inflammation in the gingival tissue in touch with the edges of the film consisting of 100 % polylactic acid.

The bio-degradable /absorbable high-molecular materials of the present invention have the following advantages in comparison with the highmolecular materials which are neither degradable nor absorbable in a living body.

According to the Guided Tissue Regeneration Technic proposed by Professor S. Nyman et al (University of Gothenburg), it is essentially required to remove the material inplanted in the periodontium immediately after the periodontium are found to be healed by such imp:Lant. For such removal, it is again necessary to perform an operation. With the biodegradable/absorbable high-molecular materials of the present invention, however, it is unnecessary to perform a reoperation, thus easing a patient of pain and relieving an economical burden to considerable degrees.

The material implanted in the periodontium is required to have strength at the beginning, but is rather needed to lose that strength after the healing of the periodontal disease. No change in strengh tends to induce inflammation. However, the bio-de gradable /absorbable high-molecular materials of the present invention have strength at the start, which can be decreased gradually or sharply with the lapse of time, and so there is no possibility of inducing inflammation in the periodontium.

Moreover, the bio-degradable/absortable high-molecular materials of the present invention have the following advantages in comparison with those consisting of homopolymers of 100 % polylactic acid.

The dynamic/mechanical properties suitable for the conditions of the periodontium can be given to the bio-degradable/absorbable highmolecular materials of the present invention because the materials Z.

A consist of the copolymers of lactide/e -caprolactone or lactide/glycolide. It is required to vary the rates of biodegradation and -absorption of the material nplanted in the periodontium depending upon the degree of periodontal disease. Especially when it is intended to decrease sharply the dynamic /mechanical properties of the bio-degradable /absorbable highmolecular materials at the time when a certain period of time elapses after its Inplant in the periodontium, difficulty is involved in freely varying the rate of hydrolysis of the bio-degradable/absorbable high- molecular material consisting of the homopolymer of 100 % polylactic acid. With the bio-degradablelabsorbable high-molecular materials of the present invention, however, it is possible to freely control their rates of degradation and absorption.

Further, the bio-degradable/absorbable high-molecular materials of the present invention give little or no physical stimuli to the soft tissues of a living body because their glass transition temperature is in the vicinity of body heat in comparison with the biodegradable/absorbable materials consisting of the homopolymer of 100 polylactic acid.

i 4 1 1 i

Claims

Claims: -

1. A periodontium-regenerating' material for the regenerative treatment of the periodontium, which is a bio-degradable/absorbable high-molecular material.

2. A periodontium-regenerating material as claimed in Claim 1, wherein a copolymer of lactidels -caprolactone or lactide/glycolide is used as said bio-degradable/absorbable high-molecular material.

3. A periodontium-regenerating material as claimed in Claim 2, 19 wherein said copolymer of lactide/s -caprolactone or lactide/glycolide has a weight-average molecular weightAn a range of 40,000 to 500,000.

4. A periodontium-regenerating material as claimed in Claim 2 or -3, wherein said copolymer of lactide/c-caprolactone or lactide/glycolide has a molar ratio in a range of 95:5 to 5:95.

5. A material as claimed in any of claims 2 to 4, wherein said copolymer of lactide/e-caprolactone or lactide/glycolide is in the form of a film or a sheet having a thickness in a range of 10 to 500 pm.

6. A material as claimed in any of claims 2 to 5, wherein said copolymer of lactide/ c - caprolactone or lactide /glycol ide is in the form of a porous film or sheet.

7. A material as claimed in any of claims 2 to 6, wherein said copolymer of lactide/F,-caprolactone or lactide/glycolide has a dynamic modulus of elasticity in a range of 5 x 107 to 5 x 109 dynes/cml and anelongation rate of 100 to 2,000 %, both measured at room temperature (25 C).

8. A material as claimed in any of claims 2 to 7, wherein said copolymer of lactide/E -caprolactone or lactide/glycolide has its retention rate of tensile strength reduced to zero after the lapse of one to six months due to hydrolysis action in vitro in a phosphate buffer solution of 37 'C and pE 7.4.

9. A periodontium-regenerating material substantially as described in any of Examples 1 to 4.

C Publiahed 1990 at The Patent Otftce.StLte House.801-7 t F-4h Holburn. 14ndonWC1R4TP. Purther copies Maybe Obtamed, from The PatentOfflos. Sales Branch. St Mary Cray. Orpzz4%cin. Ksnt'6R5 3RD. Printed by Multiplax tealiniques ltd. St Mary Cray. Kent, CA)zk. V87