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Clinics

Print version ISSN 1807-5932On-line version ISSN 1980-5322

Clinics vol.63 no.6 São Paulo  2008

http://dx.doi.org/10.1590/S1807-59322008000600016 

BASIC RESEARCH

 

In vitro and in vivo evaluation of lyophilized bovine bone biocompatibility

 

 

Carlos Roberto GaliaI; Carlos Alberto MacedoI; Ricardo RositoI; Tielle Muller de MelloII; Lourdes Maria Araújo Quaresma CamargoIII; Luis Fernando MoreiraI

ISchool of Medicine, Universidade Federal do Rio Grande do Sul (UFRGS) - Porto Alegre/RS, Brazil
IISchool of Biological Sciences, Pontifícia Universidade Católica do Rio Grande do Sul (PUCRS) - Porto Alegre/RS, Brazil
IIITissue Bank, Hospital de Clínicas de Porto Alegre (HCPA) - Porto Alegre/RS, Brazil. Email: cgalia@hcpa.ufrgs.br Tel.: 55 51 2101.8628 / 9986.4469

 

 


ABSTRACT

INTRODUCTION: The use of bone grafts in orthopedic, maxillofacial and dental surgery has been growing. Nevertheless, both fresh autografts and frozen allografts have limitations, and therefore, alternative synthetic or natural biomaterials, such as processed and lyophilized bovine bone graft have been developed.
OBJECTIVE: To evaluate in vitro and in vivo biocompatibility of lyophilized bovine bone manufactured in a semi-industrial scale, according to a modifical protocol developed by the authors.
METHODS: Samples of bovine cancellous bone were processed according to a protocol developed by Kakiuchi et al., and modified to process samples of bovine cancellous bone. The following trials were performed: in vitro cytotoxicity, in vivo acute systemic toxicity, in vivo oral irritation potential, in vitro pyrogenic reaction, and bioburden.
RESULTS: The in vitro evaluation of lyophilized bovine cancellous bone revealed an absence of cytotoxicity in 100% of the samples. Regarding in vivo evaluation of acute systemic toxicity, neither macroscopic abnormalities nor deaths were noted in the animals. Pyrogenicity was not greater than 0.125 UE/ml in any of the samples. The bioburden revealed negative results for microbial growth before sterilization. Regarding the oral irritation potential, in vivo evaluation at 24 and 72 hours showed that the animals had no edema or erythema on the oral mucosa.
CONCLUSION: The protocol changes established by the authors to prepare lyophilized bovine cancellous bone at a semi-industrial scale is reproducible and yielded a product with excellent biocompatibility.

Keywords: Surgery; Materials testing; Toxicity tests; Freeze drying; Bone transplantation.


 

 

INTRODUCTION

The use of bone grafts in orthopedic, maxillofacial and dental surgeries has been growing.1 Fresh autografts remain the standard option because of their structural properties, absence of immune response, and osteoinductive, osteoconductive and osteogenic properties. However, disadvantages such as longer surgical times, low availability and morbidity have limited their use.2,3

Frozen allografts have also been widely used and are considered an excellent alternative since there is virtually no site morbidity, but availability is limited; and, although rare, transmission of infectious and tumoral diseases may be associated.4-6

Therefore, alternative synthetic or natural biomaterials such as processed and lyophilized bovine bone grafts, as well as different bone processing and storage methods, have been developed and extensively studied. Bovine grafts have almost unlimited availability and great physical and chemical similarity to human bone. One of the disadvantages of bovine bone is the fact that it is a xenograft and, therefore, may trigger unwanted immunological and inflammatory host reactions host. Many efforts to develop an optimal protocol have been attempted including physical and chemical processing methods to minimize risks and to substantially decrease antigenicity, thus rendering bovine bone an acceptable alternative to autografts and allografts.7-10

One of the most important phases in the development and biological validation of biodegradable materials is the performance of rigorous clinical and experimental in vitro and in vivo trials to determine and confirm biocompatibility and bioactivity.11-13

Data obtained in these studies may determine whether the material meets the biocompatibility standards for implantable medical products. Methods and standards to evaluate the biocompatibility of these products are described in the ISO 10993-11 series of international norms.14 The ISO norms have exceeded several attempts and international agreements aimed at standardizing the evaluation of medical product safety and have been incorporated in several studies.15

This study evaluated the biocompatibility of lyophilized bovine bone manufactured in a semi-industrial scale according to a novel preparation process developed by the authors. The following assessments were performed: in vitro cytotoxicity, in vivo acute systemic toxicity, in vivo oral irritation potential, in vitro pyrogenic reaction, and bioburden.

 

MATERIALS AND METHODS

Samples

Samples of bovine cancellous bone were processed according to a protocol developed at the Osaka University, Japan16 with modifications to decrease fat content, to improve purification of the bone graft, and by use of chemical reagents capable of inactivating viruses17,18 and possibly prions.19,20 The modifications were as follows: (1) the time of graft exposure to chloroform and methanol was increased to approximately 25 days; (2) grafts were washed using an ultrasonic washer to optimize removal of organic residues, (3) immersed in hydrogen peroxide for 1h (10, 20 and 30 volumes), and (4) plunged into sodium hypochlorite. Finally, (5) the bones were cut in different shapes and granulations, were lyophilized, packed and sterilized by gamma radiation.

The 30 x 20 x 10 mm graft samples were sent to the laboratory in double packages made of surgical paper and PVC film, containing a chemical radiation dosimeter, and only those samples selected to determine bioburden were sent to the laboratory before sterilization.

The tests described below were performed by outside independent laboratories that also perform biologic, microbiologic physical and chemical tests for the pharmaceutical, medical and hospital industries. These laboratories have nationally and internationally Good Laboratory Practices Accreditation and are approved by the Brazilian Network Laboratories for Health Analysis (Rede Brasileira de Laboratórios Analíticos em Saúde - REBLAS) to perform biologic and microbiologic tests. The tests were performed at three distinct different laboratories in São Paulo, SP Brazil.

In vitro evaluation of cytotoxicity

Cell culture: The NCTC Clone 929 lines of mouse fibroblast cells (ATCC CCL-1) were used. Cells were grown in minimal Eagle medium supplemented with 10% fetal bovine serum (MEM + 10% FBS). Cells were maintained at 36ºC and dispersed using 0.2% trypsin and 0.02% EDTA (TE). After dispersion, cells were resuspended in MEM and placed in bottles as control cells and on Petry dishes for agar diffusion.21,22

Three test samples containing processed and lyophilized bovine cancellous bones in a solid, liquid or powder state underwent extraction, which was performed with saline or cottonseed oil at 37ºC for 24h and at 50ºC for 72h.

A negative control group was composed of nontoxic filter paper disks 0.5 cm in diameter, and a positive control group was composed of toxic latex fragments measuring 0.5 x 0.5 cm.

Agar diffusion: The NCTC L929 cells lines were grown as described above, seeded on Petri dishes at a concentration of about 3 x 105 cells/ml, and were incubated for 48h at 37ºC in a 5% CO2 humidified incubator to form a monolayer. The liquid culture medium was replaced with a solid medium composed of equal parts of double-concentrated MEM medium and BBL agar (BD) containing 0.1% neutral red vital stain (USP XXIII/2005, ISO 10993-5). The solid samples were placed directly on the solid agar medium; the liquid samples were poured on nontoxic filter paper disks and placed on the medium; and the powder samples were placed in a cylinder fixed above the medium. The dishes were incubated again for 24h. The samples were evaluated macro- and microscopically, and cytotoxicity was confirmed when a halo was found under or around the test sample. Halo diameters were measured, in quadruplicate and a mean value was calculated and subtracted from the diameter of the nontoxic filter paper disks used to soak the samples to obtain the zone index (ZI), which is the unstained area by the vital stain. ZIs were scored from zero to four, where zero corresponds to no halo under or around the sample, and four corresponds to a halo greater than 1.0 cm around the sample. Cytotoxicity values were correlated to the ZI scores of each sample, varying from absent to severe cytotoxicity.21,23

In vivo evaluation of acute systemic toxicity

Animals: Twenty Albino Swiss male mice with a mean weight of 20 g divided into two groups were used for this study.

Tests: Different media and administration routes were used for each group of ten animals. In group 1, cotton seed oil was used as the medium for the intraperitoneal injection, while in group 2, non-pyrogenic sterile saline was used for intravenous injection. On each group, five animals were considered for tests or as controls. The intraperitoneal substrate for injection that were produced in an autoclave at 121ºC for 1h.

In group 1, animals were intraperitoneally injected with 1.0 ml /20 g body weight of sterile cotton seed oil (batch no. 103K0064). Animals in the test subgroup received 1.0 g of bone sample per 20.0 ml of cotton seed oil, and the control subgroup received only sterile cotton seed oil.

In group 2, animals were intravenous injected with 1.0 ml/20 g body weight of non-pyrogenic sterile saline. Animals in the test subgroup received 1.0 g of bone sample per 20.0 ml of non-pyrogenic sterile saline solution (batch no. 060406Ql001), while the control subgroup only received non-pyrogenic sterile saline.

All animals were treated with disposable sterile syringes and needles, and were controlled for body weight, macroscopic changes, and number of deaths at 4, 24, 48 and 72h. The animals were kept in special cages in the laboratory facility and received mouse chow and water ad libitum, specific care, such as light-dark cycles, room temperature and noise control, by the veterinarians and biologists involved in the study.24

In vivo evaluation of the oral irritation potential

Animals: Twelve Male Cavia porcellus (Guinea pigs) (mean weight = 570 g) were used. The animals were kept at 18 to 21ºC at 64% humidity and 12-hour light-dark cycles (12LD).

Tests: Two groups of six animals were divided in a test group and a show-treated (controls) group. The extract was prepared at a concentration of 0.2 g of bone sample per ml of deionized water and incubated at 121ºC for 1h.

The extract was applied for 10 consecutive days on the oral mucosa of the six animals in the test group. Before application, the mucosa of each animal was daily examined macroscopically by a distinct technician than that one who had applied the extract, and changes if any were recorded. Only deionized water was applied to the oral mucosa of, all animals in the control group.

For the final classification of the extract, the criterion of the Brazilian Institute of Health Quality Control (Instituto Nacional de Controle de Qualidade em Saúde - INCQS) was used. The arithmetic means of readings for edema and erythema were calculated at 24 and 72h. Thus, an index was calculated by the average of four means - two readings per day in two reading days.

In vitro evaluation of pyrogenicity

The Limulus Amebocyte Lysate (LAL) assay (batch no. FL 0842) of 0.125 UE/ml (unit of endotoxin per ml) sensitivity was used for qualitative evaluation of endotoxins produced by the bone samples if any. A mixture of 0.1 ml LAL and 0.1 ml of the extract was prepared in a test tube.

The mixture was immediately incubated for 1h at a controlled temperature of 37ºC. After that, the tubes were removed and checked for a fixed gel formation that did not slide when the tube was positioned upside down. This method was based on the chain reaction between the bacterial endotoxin and a protein component of LAL, which produces an easily identifiable opaque gel. The formation of a gel in the bottom of the tube indicated a positive response for endotoxin production by the sample, in an amount equal to or greater than A lysate of 0.125 UE/ml sensitivity value as specified on the reagent label. Since was considered negative (<0.125 UE/ml) no gel formation can be observed.

Determination of microbial load (bioburden)

To determine the microbial load before sterilization, the extract were labeled, placed in double blister packs and sent for analyzes to the three distinct laboratories involved in the study. For each of the three samples, a pool of granulate samples was prepared and diluted in 0.9% sterile saline at a 1:10 ratio. Serial dilutions were plated in tryptic soy agar (TSA) and incubated at 35ºC for 24-48h to read the total aerobic mesophiles. Serial dilutions were also plated in Sabouraud agar and incubated at 25ºC for 5 days to read the total filamentous fungi. At those time points, colonies of 30-300 colony forming units (CFU/g) were counted.

 

RESULTS

In vitro evaluation of cytotoxicity potential

In vitro evaluation of lyophilized bovine cancellous bone showed no cytotoxicity potential in 100% of the samples. There were no statistically significant differences between control groups (nontoxic filter paper disks 0.5 cm in diameter) and test group containing sample of lyophilized bovine cancellous bone. ZI scores were zero; that is, there were no stained areas under or around the samples. There was, however, a statistically significant difference between these groups and the positive control group, which had a ZI of 4, indicating a stained area greater than 1.0 cm around the sample (Table 1).

 

 

In vivo evaluation of acute systemic toxicity

During the study, all mice in the test subgroup of group 1 had a mean weight gain of 0.5 g (from 20.7 g to 21.2 g), and the animals in the control subgroup had a mean weight gain of 0.6 g (from 21.9 g to 22.4 g); In group 2 of intravenous injections, animals in the test subgroup had a mean weight gain of 0.5 g (from 20.1 g to 20.6 g) and controls had a mean weight gain of 0.6 g (from 22.3 g to 22.9g); these differences were also not statistically significant.

No macroscopic abnormalities were noted and there were no deaths in either of the subgroups (Table 2 and 3).

 

 

In vivo evaluation of the oral irritation potential

No significant changes in weight or general conditions were found in the negative control group or in the test group. Observations on the test and control groups at 24 and 72h showed that none of the Guinea pigs had edema or erythema on the oral mucosa.

Evaluation of pyrogenicity

All samples showed a negative pyrogenic result, since lysates were <0.125 UE/ml and no gel formation occurred.

Determination of microbial load (bioburden)

The tests to determine product bioburden showed negative results for microbial growth before sterilization. The physical and chemical processing procedure applied to the bovine cancellous bone samples resulted in a product free of aerobic mesophilic bacteria, filamentous fungi and yeast.

 

DISCUSSION

The low availability and inherent risks associated with the use of bone autografts and allografts have led several researchers to study and develop alternative bone substitutes, such as calcium phosphate ceramics and lyophilized animal bone grafts. Several products have been developed, and processing and production methods have improved.9, 25

In this study, we used lyophilized bovine bone grafts produced by modifying a protocol originally developed by Kakiuchi et al.16 at Osaka University, Japan to minimize mechanical, physical and chemical changes, to reduce fat content, and to increase purity of the bone graft. Therefore, for analytical purposes, it is very similar to deep-frozen, unprocessed bone allografts.9 Private companies participated in improving this technique because of the large scale required for industrial production.

Evaluating the biologic safety of a medical product is part of the process of risk management and analysis. Tests must be selected according to the type of contact that the product will have with the host (i.e., superficial, external or implantable), the nature of the place in which the product will be applied, and the length of contact between the product and host.11-13,26

Quantitative or qualitative biocompatibility tests are quick and have been simplified, turning into systematic, detailed and safe procedures. Analyzis of material properties is currently a common practice in the industrial when both, adapting new production methods and analyzis of final products are considered. In some cases, these tests may preclude the performance of other biologic tests.15

Systemic toxicity studies evaluate potential adverse effects of medical products on other tissues and organs other than those caused at the initial contact. These tests evaluate the effects that any substance released by the implantable product may have on the host general health or organs, such as liver, heart, kidneys or brain.14

The ISO 10993-11 norm,14 which is pliable in terms of study designs to investigate such effects, has established systematic international testing norms that have increased the safety of biomedical products. Study protocols should be based on classic toxicological evaluations of drugs and other chemical substances. However these protocols should be modified to evaluate solid components on medical products.27 The product tested in our study did not show any systemic reaction, confirming its biocompatibility, an essential requirement for its use.

The in vitro cytotoxicity test is a fast, standardized, sensitive and low-cost test to determine whether a material contains significant amounts of extractable substances that may harm the host. The results of our in vitro cytotoxicity tests, which prevent the use of experimental animals, showed a good correlation with those reported on in vivo studies of short-term implants.27 The results of cytotoxicity tests showed that the end product did not have any toxic potential that might cause reactions in surromding tissues after implantation i.e., no toxic substance was released by the processed bone, as well as no chemical residue was found at significant levels that might cause tissue damage.

The oral mucosa irritation test focused on whether the product would cause irritation when in contact with the oral mucosa of Guinea pigs, a useful model, to determine changes and lesions that may affect the stratified epithelium.28 The results of our study indicated that the bone product under analysis showed no mucosa harm further supporting itsbiosafety.

Contamination with bacterial endotoxins (pyrogenic substrates) is often associated with fever, but other substances released by distinct materials may also cause this side effect.

An evaluation of the pyrogenic potential of a material is typically included in biocompatibility studies. Pyrogenic reactions due to contamination by endotoxins are closely associated with the manufacturing processes, and assessment of contamination is part of the routine measures of production control of any material.29 This study showed that our end product was pyrogen-free, particularly free of bacterial endotoxins or other substances that might cause fever when released.

The efficiency of a product sterilization depends on the type and number of microorganisms (bioburden) found in that product. Therefore, knowing the microbial load before sterilization helps to determine parameters for sterilization and to plan a more adequate and shorter, less intense sterilization than when the process is based on an arbitrary number of organisms. Implantable products belong to the group of medical health products that require control of the microbial load acquired during manufacture and handling.30 A simple method to determine bioburden should be used not only for routine examination of end-products before sterilization but also to provide manufacturers on important data for designing and controlling production processes, particularly considering major sources of contamination.31

Our tests to determine product bioburden showed that our product had a very low microbial load and this information was consided to define and validate the sterilization process to be used in this product. Additionally, the risks associated with the original characteristics of the product and its microbial load, the selection of an appropriate sterilization method should also consider the production process, the product itself and purpose.32

After evaluating the results of bioburden tests, a minimum irradiation dose was defined for sterilization. and by using a pharmaceutical sterilization test, the dose of 20 kGy was then validated considering a safety margin to irradiate the product.33 Of the microorganisms already associated with human bone grafts, all, but anaerobic spores, are highly sensitive to gamma radiation. Several reports showed that high radiation doses (greater than 25 kGy) affect the mechanical properties of bone.34 Therefore, the use of lower doses, combined with cleaning and inactivation methods or the use of preserving radiation, may safely sterilize bone assuring maintenance of functional, chemical and structural properties.35,36

 

CONCLUSIONS

In vivo and in vitro tests showed that lyophilized bovine cancellous bone prepared at a semi-industrial scale according to a protocol developed by the authors is a reproducible product with excellent biocompatibility.

 

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Received for publication on July 18, 2008
Accepted for publication on August 5, 2008

 

 

Galia CR, Macedo CA, Rosito R, Mello TM, Camargo LMAQ, Moreira LF. In vitro and in vivo evaluation of lyophilized bovine bone biocompatibility. Clinics. 2008;63:801-6.

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