US 20060269892 A1
Orthodontic methods comprise applying force to reposition teeth and administering a tissue remodeling and/or an angiogenic substance(s) to the periodontal tissue surrounding the teeth to be moved. The substance(s) may be delivered before, during, or after the teeth are moved, and the substance(s) may be selectively applied only to those teeth undergoing movement at any particular time. The substance(s) may be applied from the dental repositioning appliance or may be applied separately, either topically or by injection.
1. A method for enhancing tooth mobility or stability, said method comprising administering a tissue remodeling and/or angiogenic substance(s) to a living host.
2. A method as in
3. A method as in
4. A method as in
This application is a continuation of application Ser. No. 10/695,299, filed on Oct. 27, 2003, which claims the benefit of U.S. Provisional Application No. 60/423,026, filed on Nov. 1, 2002, the full disclosures of which are incorporated herein by reference.
1. Field of the Invention
The present invention relates generally to medical apparatus and methods. More particularly, the present invention relates to methods and systems for facilitating, accelerating, and stabilizing tooth movement before, during and after orthodontic procedures.
Orthodontic procedures suffer from four major problems. First, the braces or other appliances which effect the tooth movement must be worn for long periods of time. Second, even after a successful orthodontic treatment, the teeth often relapse towards their original positions once the braces or other treatment appliances are removed. Third, the mechanically induced movement of teeth can cause significant discomfort to the patient. Fourth, the wearing of braces is esthetically displeasing, uncomfortable, and compromises oral hygiene. While recently introduced clear plastic visible “aligners” largely overcome the latter problems, such aligners are not suitable for all patients. Moreover, the aligners do not reduce treatment time, do not reduce the risk of relapse, and do not lessen the pain associated with tooth movement in the jaw.
For these reasons, it would be desirable to provide improved orthodontic technologies for moving teeth which overcome at least some of the problems noted above. In particular, it would be desirable to provide orthodontic methods and systems which can reduce the time necessary to effect a desired tooth movement, which can reduce the pain associated with tooth movement, which can reduce the tendency of teeth to relapse to their original positions after the orthodontic treatment is stopped, and/or which can reduce the time in which unsightly braces need to be worn.
2. Description of Background Art
Nicozisis et al. (2000) Clin. Orthod. Res. 3:192-201, describes experiments which demonstrate the presence of endogenous relaxin in cranial tissue of mice and speculates that relaxin may be used as an adjunct to orthodontic or surgical therapy to promote manipulation of sutural tissues or affect stability. The application of electrical current to stimulate bone growth and remodeling in orthodontic procedures is described in U.S. Pat. Nos. 4,854,865; 4,519,779; and 4,153,060. Appliances for local and systematic drug delivery to the gingival tissues are described in U.S. Pat. Nos. 6,159,498, 5,633,000; 5,616,315; 5,575,655; 5,447,725; 5,294,004; 4,959,220; 4,933,183; 4,892,736; 4,685,883; and Re. 34,656. Polymeric shell appliances for repositioning teeth are described in U.S. Pat. No. 5,975,893. The full disclosures of each of the above U.S. patents are incorporated herein by reference.
The present invention provides improved methods and systems for repositioning teeth in patients. In addition, the present invention provides improved methods and systems for stabilizing teeth which have already been repositioned in order to reduce or eliminate the tendency of the repositioned teeth to relapse, i.e., move back toward their prior positions. The methods for repositioning teeth comprise applying force to at least one tooth, and typically to more than one tooth and/or to different teeth over time, in the jaw of the patient. For both repositioning or stabilizing, tissue remodeling and/or an angiogenic substance(s) is administered to the patient to promote remodeling of periodontal tissue surrounding the root(s) of the tooth or teeth to be moved. Preferred substance(s) will bind to and activate the relaxin receptor in the tissues which anchor the teeth or other craniofacial structures. Most preferred is relaxin or an analog or mimetic thereof which combines tissue remodeling activity with angiogenic activity. Analogs include peptides, oligomers, fragments, etc. which comprise the active region of native relaxin and mimetics include small molecule drugs, typically below 2 kD, designed to mimic the activity of native relaxin. Alternatively, substance(s) with predominantly angiogenic activity could be selected, such as VEGF, bFGF, estrogen, nitrous oxide, naltrexone, or the like. Further alternatively, collagenases or other tissue-softening enzymes could be utilized to promote periodontal tissue remodeling according to the present invention. In some instances, it may be desirable to combine two or more tissue remodeling and/or angiogenic substance(s) having differing activities. In other instances it may be desirable to deliver different tissue remodeling and/or angiogenic substance(s) at different times during the orthodontic treatment and/or to different regions of the periodontal tissue.
The term “relaxin” means human relaxin, including intact full length relaxin or a portion of the relaxin molecule that retains biological activity [as described in U.S. Pat. No. 5,023,321, preferably recombinant human relaxin (H2)] and other active agents with relaxin-like activity, such as Relaxin and portions that retain biological activity Like Factor (as described in U.S. Pat. No. 5,911,997 at SEQ ID NOS: 3 and 4, and column 5, line 27-column 6, line 4), relaxin analogs and portions that retain biological activity (as described in U.S. Pat. No. 5,811,395 at SEQ ID NOS: 1 and 2, and column 3, lines 16-40), and agents that competitively displace bound relaxin from a receptor. Relaxin can be made by any method known to those skilled in the art, for example, as described in any of U.S. Pat. Nos. 5,759,807; 4,835,251 and co-pending U.S. Ser. No. 07/908,766 (PCT US90/02085) and Ser. No. 08/080,354 (PCT US94/0699).
The tissue remodeling and/or angiogenic substance(s) will be delivered at a delivery rate and a total dosage which are selected to facilitate tooth repositioning and tissue remodeling. Typically, the dosage rates will be in the range from 1 ng to 500 μg per day, usually from 10 ng/day to 20 μg/day, preferably from 20 ng/day to 10 μg/day. The dosage and other aspects of the delivery may be adjusted from time-to-time in response to the effectiveness of treatment, such as the resistance of a particular tooth or group of teeth, where the dosage might be increased if resistance is not sufficiently reduced in response to an initial dosage.
The substance(s) may be delivered at any point during the orthodontic treatment where tooth repositioning and/or tissue remodeling may be promoted. For example, the substance(s) may be applied prior to any application of force intended to move the teeth. Additionally or alternatively, the substance(s) may be applied during all or any portion of the time during which force is being applied to move the teeth. Further additionally or alternatively, the substance(s) may be applied after the teeth have been repositioned to a final desired configuration. In the latter case, application of the substance(s) may be particularly effective for promoting tissue remodeling in order to reduce the risk of relapse. In such instances, the substance(s) may be delivered using retainers or other appliances intended to help maintain the teeth in their desired final configuration. When being delivered to inhibit relapse, the remodeling and/or angiogenic substance(s) may be delivered for a limited period of time in a limited period before and/or immediately following the end of the orthodontic procedure or may be delivered continuously or periodically for long periods of time or indefinitely following the end of the orthodontic procedure. For example, the substance(s) may be delivered to some or preferably all of the regions of the gingiva where teeth have been moved in order to promote stabilization and remodeling of the tissue, usually over a period of one to eight weeks, more usually two to six weeks prior to the end of treatment.
The teeth may be repositioned by any conventional orthodontic appliance intended for applying force to move teeth. In particular, the present invention is compatible with both the use of wire and bracket systems, commonly referred to as “braces,” as well as with newer systems employing removable appliances for repositioning teeth, such as the Invisalign® System, available from Align Technology, Inc., Santa Clara, Calif., and the “red, white, and blue” system available from Sybron Dental Specialties, Irvine, Calif. The present invention will also be useful with dental “positioners” which are elastomeric appliances having pre-formed tooth-receiving cavities where the patient bites into the elastomeric appliance in order to force tooth movement. Finally, the present invention may be used with dental retainers which are polymeric shell appliances typically used to maintain a final, desired tooth configuration and prevent relapse. When used with dental repositioning appliances of any type, the application of the tissue remodeling and/or angiogenic substance(s) according to the present invention will usually both facilitate tooth movement by modifying the tissue structures within the periodontal tissue which anchor the teeth and also promoting tissue remodeling which allows such tissue structures to accommodate the repositioned teeth with less tendency toward relapse.
The substance(s) of the present invention may be applied and administered in a wide variety of ways. Most simply, and as presently preferred, the substance(s) could be “painted” or otherwise topically applied to the patient's gingiva using a conventional single-use applicator such as a swab, brush, syringe, or the like. The substance(s) may be prepared in a conventional form of topical composition, such as a gel, cream, ointment, or other fluid or liquid substance. Alternatively, the substance(s) could be administered by injecting into the periodontal tissue. Additionally, the substance(s) could be delivered using a patch or other appliance which is worn on the teeth or gingiva, optionally being formed as part of the same appliance which is used to move the teeth, e.g., a bracket or removable shell appliance or retainer. In such instances, the substance(s) may be incorporated into conventional drug reservoirs which both maintain a supply of the substance(s) and which release the substance(s) at a controlled rate, over time, to target sites on the gingiva. Suitable drug delivery structures for delivering the substance(s) to the patient gingiva are described in the patent and medical literature, see, e.g., U.S. Pat. Nos. 6,159,498, 5,575,655; 5,194,003; 4,933,182; and 4,685,883, the full disclosures of which are incorporated herein by reference.
In some instances, it may be desirable to provide for enhanced penetration of the substance(s) into the gingival. For example, the substance(s) could be formulated with tissue penetration or permeation enhancers, such as dimethylsulfoxide (DMSO). Alternatively or additionally, the substance(s) can be delivered while applying energy in a manner to promote tissue penetration, including the application of an electric current in order to achieve electroporation or iontophoresis, and/or the application of ultrasound energy. The currents needed to provide for electroporation are relatively low, typically around 0.1 mA can be provided by batteries contained within the delivery structure or alternatively by external structures which are periodically applied to the gingiva or appliances present over the gingiva. Similarly, ultrasound-enhanced substance delivery can be effected by transducers incorporated into the delivery appliances and/or provided by external appliances. Suitable ultrasound conditions are from 20 kHz to 100 kHz at energy levels of one to ten J/cm2.
A particular advantage of the present invention is that particular teeth can be treated with the substance(s) while other teeth in the same jaw remain untreated. In this way, those teeth which are to be moved at any point during the course of orthodontic treatment may be “relaxed” and prepared for movement while other teeth which are needed as “anchor teeth” remain untreated. In this way, the wire and bracket system, removable aligner, or the like, may be anchored on those teeth which have not been treated with the substance(s), while those teeth which are intended to be moved may be treated and more readily moved. Of course, during a normal orthodontic treatment, different teeth will be targeted for movement at different times. The present invention allows only those teeth which are intended to be moved at any particular time to be treated at that time while other teeth in the dentition remain untreated during that time and available as anchor teeth for performing the orthodontic treatment.
The present invention may also advantageously be combined with other orthodontic treatment protocols, such as electroosteogenesis where a small electrical current is applied to the gingiva or jaw to stimulate the tissues. It is believed that the combination of the substance(s) with such electroosteogenesis could provide tooth movement which is improved over that achieved with either approach alone. Moreover, the application of the electric current might act to provide “electroporation” and enhance the uptake of the substance(s) into the periodontal tissues, as described above.
In a further aspect of the present invention, improved orthodontic treatment methods are provided. The orthodontic treatment methods are of the type where at least one tooth in a patient jaw is repositioned. The improvement comprises administering at least one tissue remodeling and/or an angiogenic substance to the patient before, during, or after the force has been applied. The preferred aspects of this method are generally the same as described above.
The present invention still further provides oral delivery appliances comprising a structure and a tissue remodeling and/or an angiogenic substance(s). The structure is mountable on or over at least a portion of a patient gingiva, and the substance(s) is carried by the structure so that said substance(s) is release into at least a region of the gingiva while the structure is mounted on or over the gingiva. Typically, the delivery appliance mounts over the gingiva of an entire jaw, but in some instances it may mount over the gingiva of less than the entire jaw. Typically, the structure will include at least a portion which engages or mounts over the gingiva adjacent the roots of the target teeth, typically from one to twelve teeth, usually from one to six teeth, often from one to five teeth, and sometimes only a single tooth. The appliance may be in the form of a patch which adheres to the gingiva, a shell which is removably placeable over the teeth in the gingiva, or the like. The use of patches for delivery of the substance(s) may be particularly advantages since the patches can be cut to size in order to control dosage and/or delivery area to the gingiva. Such modified patches may be applied or adhered directly to the gingiva or alternatively may be positioned beneath a retainer which is worn to maintain the positions of the teeth. When wire and bracket orthodontic appliances are used, the delivery appliance may be formed to mount on the wire or onto the bracket, may be incorporated as part of the bracket or wire, or may be some combination thereof. The relaxin or other tissue remodeling and/or angiogenic substance may be incorporated into the oral delivery appliance in a variety of ways. Most commonly, the relaxin will be in a liquid, gel, or other releasable form which is incorporated into a time-release structure to apply the substance to the gingiva at a desired dosage rate. For example, the substance(s) may be incorporated into a porous structure and/or in a reservoir which is covered by a porous structure. In either case, the porous structure acts as a rate-controlling membrane or barrier to achieve the desired delivery rate. Alternatively, the substance(s) may be present in a biodegradable matrix which degrades in the oral environment over time to achieve a desired release rate of the substance. Suitable degradable substances include polymers, such as glycolic acid polymers and related materials.
In a still further aspect of the present invention, topical oral compositions comprise a carrier and a tissue remodeling and/or an angiogenic substance(s). The carrier is of the type which may be topically applied to a patient's gingiva, typically being in the form of a gel, cream, ointment, microemulsion or other liquid. The tissue remodeling and/or an angiogenic substance(s) may be any of the substance(s) listed above. The composition may be provided in any conventional applicator, such as a tube, syringe, bottle, or the like, and will be maintained in a sterile condition within the applicator.
The present invention provides improved and facilitated orthodontic treatment by delivering tissue remodeling and/or an angiogenic substance(s) to periodontal tissue in which the teeth to be moved are rooted or anchored. As used hereinafter, “periodontal tissue” will refer to the connective tissue within the periodontal tissues, specifically including the tissue and ligaments which anchor the teeth in the bone. The application of the tissue remodeling and/or an angiogenic substance(s) to the periodontal tissue will both loosen the tissue and ligaments as well as promote remodeling of the tissue during and after orthodontic treatment.
The tissue remodeling and/or angiogenic substance(s) may be delivered to the periodontal tissue in a variety of ways, including systemic delivery, local injection, local topical application, continuously, periodically, and combinations thereof. Topical delivery is presently preferred and may be achieved using a conventional surface applicator, such as a brush, swab, syringe, squeeze tube, sponge, or other similar device. Alternatively, topical delivery may be effected using various controlled release devices, such as retainers, patches, orthodontic brackets and wires, and other appliances which may be positioned on or over the teeth and which have been modified in order to release the substance(s) to the gingiva. In some cases, it will be desired to deliver the drug into the gingival margin which is the line or groove along the gingiva-tooth interface. Substances may be applied as part of formulations which are delivered over the gingiva and/or into the sulcus. In some instances, it may be desirable to plant small substance delivery structures directly into the sulcus in a manner analogous to the delivery of antibiotics using systems, such as the PerioChip® available from Dexcel Pharma. The following specific examples of patches and structures for delivering the tissue remodeling and/or angiogenic substance(s) of the present invention are meant to be exemplary and not limiting.
As shown in
Referring now to
The following examples are offered by way of illustration, not by way of limitation.
Two studies are presented, one examining properties of the periodontal and gingival tissues to relaxin and the second on dose finding.
I. In Vivo Studies of the Periodontal Ligament
A rat model was utilized because the rat has been historically used for many orthodontic studies. There were five animals per treatment group. Rats were treated for 1 or 3 days with human relaxin (H2 gene product) or vehicle control (Table 1 below). Relaxin or control vehicle was administered via Alzet implanted minipumps. In addition, relaxin treated rats received a 0.5 mg bolus injection (1.43 mg/kg) of relaxin at the time pumps were placed.
The jaws were collected for transport to the University of Washington for analysis. The day 1 jaws were delivered fresh, and the day 3 jaws were delivered frozen. Teeth from each treatment group were tested for “looseness” using a material testing device (MTD), and the periodontal ligament (PDL) was tested in a “push-out” test. The rest of the jaw was saved for histological analysis.
These tests evaluated the ability of human relaxin (H2) to accelerate tooth movement during orthodontic procedures in a rat model. These studies examined the short term effects of relaxin on tooth looseness using circulating relaxin and a material testing device (MTD).
A. Tooth Looseness Tooth displacement measured in response to a known force was measured.
B. Push-Out Test The material properties of the PDL were measured in a material testing device to obtain force/displacement curves.
C. Histological Analysis The contralateral jaw was used for histological analysis. Staining techniques were used to visualize collagen and elastin.
A. Treatment Groups Adult male Sprague-Dawley rate (89-94 days old) were purchased from Animal Technologies, Ltd, Livermore, Calif. There were five animals per treatment group having body weights of 300-350 grams. Rats were treated for 1 or 3 days with human relaxin (H2 gene product) or vehicle control (Table 1). Relaxin or control vehicle is administered via Alzet implanted minipumps. In addition, relaxin treated rats received a 0.5 mg bolus injection (1.43 mg/kg) at the time pumps were placed.
B. Relaxin Administration Human relaxin (H2) produced by Connetics, Corp was administered using Alzet osmotic pumps as previously described in the rat (Garber et al. (2001) Kidney Int. 59: 1184-85). Relaxin was administered at a rate of approximately 8 μg/kg/hr. This delivery rate has been shown to result in a blood concentration of approximately 150 ng/ml (Garber, Microchnik et al. 2001). To ensure relaxin levels rapidly achieved effective concentrations, rats were given a bolus subcutaneous injection of 0.5 mg relaxin at the time of pump implant. Control animals received the same volume of vehicle.
C. Animal Manipulations Animals were euthanized with anesthesia overdose at each of the specified time intervals. Maxillae were dissected into halves. One hemimaxilla was fixed in 10% formalin for 24 hours followed by decalcification in 10% EDTA for two weeks with daily changes of the solution, dehydration in increasing concentrations of ethanol, and embedding in paraffin for immunohistochemical and histomorphometric analyses. The other hemimaxilla was fixed, decalcified and frozen for the immunohistochemical analyses. Calvarias were saved for examination of sutures by similar procedures.
D. Measuring Tooth Movement
1. Push Out Test Gingival tissues were dissected away, and a 2 mm disk was cut through the alveolar bone and incisor (
2. Wiggle Test The second premolar tooth was embedded in paraffin and wiggled in place (
The resulting amount of displacement was measured repeatedly and averaged for each specimen.
IV. Results and Analysis
A. Material Testing The material testing of the rat jaws included two different tests. These were the “push-out” test, and the “wiggle” test. Separate teeth were used for each of these tests, as explained below. The Day I specimens were delivered fresh while the Day 3 were frozen so are only directly comparable with the controls for that day.
1. Push-Out Test The push-out test resulted in many different parameters of a stress strain curve. Several of the more relevant parameters were selected for the following graphs.
2. Tooth Wiggle Referring to
B. Histological Analysis The specimens were decalcified, embedded, sectioned and strained with a variety of histological stains. The PDL and gingival connective tissue were examined for a reduction and/or reorganization in the collagen. Collagen normally has a highly regular structure, which can be observed under a microscope using polarized light. Intact collagen demonstrates a birefringence or glow which is lost upon breakdown of the collagen.
Comparison of the treated collagen with the untreated control, under polarized label, demonstrated that the relaxin had broken down the collagen. In the relaxin treated animals, the collagen fibers have been shortened and no longer have the parallel arrangement.
V. Dose Finding Experiment
The following test helps determine an effective dose of relaxin for modification of collagen in the PDL and gingival tissues. Relaxin was administered in different doses to the rat for 5 days via Alzet subcutaneous pumps. Again the material testing device was used for measurement of the effects of relaxin. The results are shown in
The modulus is the slope of the stress strain graph. This figure suggests a dose relationship of relaxin with the softening of the PDL. It appears that even the lowest dose had modest effects on the PDL, indicating that a small amount of relaxin would be effective.
VI. Summary of Data
These data demonstrate for the first time that relaxin is effective in vivo in modifying the mechanical characteristics the ligaments that hold the tooth in the jaw. Major effects appear to be on the collagen which comprises a large portion of the PDL and gingival fibers. Relaxin affects these fibers as demonstrated by histological and physical measurements. The result of this modification of PDL and gingival fibers is to accelerate tooth movement and prevent relapse. Our data on dose indicate that even small amounts of relaxin may be effective in achieving these effects.
While the above is a complete description of the preferred embodiments of the invention, various alternatives, modifications, and equivalents may be used. Therefore, the above description should not be taken as limiting the scope of the invention which is defined by the appended claims.