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      Heparinized nanohydroxyapatite/collagen granules for controlled release of vancomycin : Heparinized nanoHA/Collagen Granules for Vancomycin Release

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          Most cited references31

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          Osteomyelitis.

          Bone and joint infections are painful for patients and frustrating for both them and their doctors. The high success rates of antimicrobial therapy in most infectious diseases have not yet been achieved in bone and joint infections owing to the physiological and anatomical characteristics of bone. The key to successful management is early diagnosis, including bone sampling for microbiological and pathological examination to allow targeted and long-lasting antimicrobial therapy. The various types of osteomyelitis require differing medical and surgical therapeutic strategies. These types include, in order of decreasing frequency: osteomyelitis secondary to a contiguous focus of infection (after trauma, surgery, or insertion of a joint prosthesis); that secondary to vascular insufficiency (in diabetic foot infections); or that of haematogenous origin. Chronic osteomyelitis is associated with avascular necrosis of bone and formation of sequestrum (dead bone), and surgical debridement is necessary for cure in addition to antibiotic therapy. By contrast, acute osteomyelitis can respond to antibiotics alone. Generally, a multidisciplinary approach is required for success, involving expertise in orthopaedic surgery, infectious diseases, and plastic surgery, as well as vascular surgery, particularly for complex cases with soft-tissue loss.
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            Biomedical applications of collagen.

            Collagen is regarded as one of the most useful biomaterials. The excellent biocompatibility and safety due to its biological characteristics, such as biodegradability and weak antigenecity, made collagen the primary resource in medical applications. The main applications of collagen as drug delivery systems are collagen shields in ophthalmology, sponges for burns/wounds, mini-pellets and tablets for protein delivery, gel formulation in combination with liposomes for sustained drug delivery, as controlling material for transdermal delivery, and nanoparticles for gene delivery and basic matrices for cell culture systems. It was also used for tissue engineering including skin replacement, bone substitutes, and artificial blood vessels and valves. This article reviews biomedical applications of collagen including the collagen film, which we have developed as a matrix system for evaluation of tissue calcification and for the embedding of a single cell suspension for tumorigenic study. The advantages and disadvantages of each system are also discussed.
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              The pharmacokinetic and pharmacodynamic properties of vancomycin.

              Vancomycin is one of only a few antibiotics available to treat patients infected with methicillin-resistant Staphylococcus aureus and methicillin-resistant, coagulase-negative Staphylococcus species. Therefore, understanding the clinical implications of the pharmacokinetic and pharmacodynamic properties of vancomycin is a necessity for clinicians. Vancomycin is a concentration-independent antibiotic (also referred to as a "time-dependent" antibiotic), and there are factors that affect its clinical activity, including variable tissue distribution, inoculum size, and emerging resistance. This article reviews the pharmacokinetic and pharmacodynamic data related to vancomycin and discusses such clinical issues as toxicities and serum concentration monitoring.
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                Author and article information

                Journal
                Journal of Biomedical Materials Research Part A
                J. Biomed. Mater. Res.
                Wiley
                15493296
                October 2015
                October 2015
                March 26 2015
                : 103
                : 10
                : 3128-3138
                Affiliations
                [1 ]i3S-Instituto de Investigação e Inovação em Saúde, Universidade do Porto; Porto 4099-002 Portugal
                [2 ]INEB-Instituto de Engenharia Biomédica; Divisão de Biomateriais; Universidade do Porto; Rua do Campo Alegre 823 Porto 4150-180 Portugal
                [3 ]Faculdade de Engenharia; Departamento de Engenharia Metalúrgica e de Materiais; Universidade do Porto; Rua Roberto Frias S/N Porto 4200-465 Portugal
                [4 ]REQUIMTE; Instituto Superior de Engenharia do Porto, Instituto Politécnico do Porto; Rua Dr António Bernardino de Almeida 431 Porto 4200-072 Portugal
                Article
                10.1002/jbm.a.35454
                0283579b-8539-4408-b826-77982e8b9e17
                © 2015

                http://doi.wiley.com/10.1002/tdm_license_1.1

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