Physiochemical properties and application of hyaluronic acid: a systematic review

Summary Background Hyaluronic acid is a widely available, biocompatible, polysaccharide with distinguishing physiochemical properties which inspire its application throughout several fields of medicine. Objective We aim to investigate the application of hyaluronic acid and its effectiveness througho...

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Vydané v:Journal of cosmetic dermatology Ročník 15; číslo 4; s. 520 - 526
Hlavní autori: Salwowska, Natalia M, Bebenek, Katarzyna A, Żądło, Dominika A, Wcisło-Dziadecka, Dominika L
Médium: Journal Article
Jazyk:English
Vydavateľské údaje: England Blackwell Publishing Ltd 01.12.2016
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ISSN:1473-2130, 1473-2165, 1473-2165
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Abstract Summary Background Hyaluronic acid is a widely available, biocompatible, polysaccharide with distinguishing physiochemical properties which inspire its application throughout several fields of medicine. Objective We aim to investigate the application of hyaluronic acid and its effectiveness throughout several fields of medicine, including several therapies administered and prescribed by general health practitioners. Methods We conducted a systematic review on randomized controlled trials about the physiochemical properties of hyaluronic acid and its application through primary care. Studies included in this review were peer reviewed and met our inclusion criteria. Findings Factors were clustered into the following: uses throughout several fields of medicine, physiochemical properties, bioavailability, tolerance, effectiveness, and adverse effects. Therapies with hyaluronic acid provided long‐lasting, pain relieving, moisturizing, lubricating, and dermal filling effect. Tissue hydration, elasticity, and durability improved. Conclusions Adjunct therapy with hyaluronic acid provides longer‐lasting therapeutic effect when compared to the use of glucocorticosteroids and NSAIDs in osteoarthritic chronic diseases, is well‐established in ophthalmology due to its lubricating properties for the corneal endothelium, and improves tissue hydration and cellular resistance to mechanical damage in aesthetic dermatology, and has marginal adverse effects. Several trials indicated its role in tumor markers, liver diseases, and in pharmaceuticals, but further research would be necessary to draw conclusive results in those fields.
AbstractList Summary Background Hyaluronic acid is a widely available, biocompatible, polysaccharide with distinguishing physiochemical properties which inspire its application throughout several fields of medicine. Objective We aim to investigate the application of hyaluronic acid and its effectiveness throughout several fields of medicine, including several therapies administered and prescribed by general health practitioners. Methods We conducted a systematic review on randomized controlled trials about the physiochemical properties of hyaluronic acid and its application through primary care. Studies included in this review were peer reviewed and met our inclusion criteria. Findings Factors were clustered into the following: uses throughout several fields of medicine, physiochemical properties, bioavailability, tolerance, effectiveness, and adverse effects. Therapies with hyaluronic acid provided long‐lasting, pain relieving, moisturizing, lubricating, and dermal filling effect. Tissue hydration, elasticity, and durability improved. Conclusions Adjunct therapy with hyaluronic acid provides longer‐lasting therapeutic effect when compared to the use of glucocorticosteroids and NSAIDs in osteoarthritic chronic diseases, is well‐established in ophthalmology due to its lubricating properties for the corneal endothelium, and improves tissue hydration and cellular resistance to mechanical damage in aesthetic dermatology, and has marginal adverse effects. Several trials indicated its role in tumor markers, liver diseases, and in pharmaceuticals, but further research would be necessary to draw conclusive results in those fields.
Hyaluronic acid is a widely available, biocompatible, polysaccharide with distinguishing physiochemical properties which inspire its application throughout several fields of medicine.BACKGROUNDHyaluronic acid is a widely available, biocompatible, polysaccharide with distinguishing physiochemical properties which inspire its application throughout several fields of medicine.We aim to investigate the application of hyaluronic acid and its effectiveness throughout several fields of medicine, including several therapies administered and prescribed by general health practitioners.OBJECTIVEWe aim to investigate the application of hyaluronic acid and its effectiveness throughout several fields of medicine, including several therapies administered and prescribed by general health practitioners.We conducted a systematic review on randomized controlled trials about the physiochemical properties of hyaluronic acid and its application through primary care. Studies included in this review were peer reviewed and met our inclusion criteria.METHODSWe conducted a systematic review on randomized controlled trials about the physiochemical properties of hyaluronic acid and its application through primary care. Studies included in this review were peer reviewed and met our inclusion criteria.Factors were clustered into the following: uses throughout several fields of medicine, physiochemical properties, bioavailability, tolerance, effectiveness, and adverse effects. Therapies with hyaluronic acid provided long-lasting, pain relieving, moisturizing, lubricating, and dermal filling effect. Tissue hydration, elasticity, and durability improved.FINDINGSFactors were clustered into the following: uses throughout several fields of medicine, physiochemical properties, bioavailability, tolerance, effectiveness, and adverse effects. Therapies with hyaluronic acid provided long-lasting, pain relieving, moisturizing, lubricating, and dermal filling effect. Tissue hydration, elasticity, and durability improved.Adjunct therapy with hyaluronic acid provides longer-lasting therapeutic effect when compared to the use of glucocorticosteroids and NSAIDs in osteoarthritic chronic diseases, is well-established in ophthalmology due to its lubricating properties for the corneal endothelium, and improves tissue hydration and cellular resistance to mechanical damage in aesthetic dermatology, and has marginal adverse effects. Several trials indicated its role in tumor markers, liver diseases, and in pharmaceuticals, but further research would be necessary to draw conclusive results in those fields.CONCLUSIONSAdjunct therapy with hyaluronic acid provides longer-lasting therapeutic effect when compared to the use of glucocorticosteroids and NSAIDs in osteoarthritic chronic diseases, is well-established in ophthalmology due to its lubricating properties for the corneal endothelium, and improves tissue hydration and cellular resistance to mechanical damage in aesthetic dermatology, and has marginal adverse effects. Several trials indicated its role in tumor markers, liver diseases, and in pharmaceuticals, but further research would be necessary to draw conclusive results in those fields.
Hyaluronic acid is a widely available, biocompatible, polysaccharide with distinguishing physiochemical properties which inspire its application throughout several fields of medicine. We aim to investigate the application of hyaluronic acid and its effectiveness throughout several fields of medicine, including several therapies administered and prescribed by general health practitioners. We conducted a systematic review on randomized controlled trials about the physiochemical properties of hyaluronic acid and its application through primary care. Studies included in this review were peer reviewed and met our inclusion criteria. Factors were clustered into the following: uses throughout several fields of medicine, physiochemical properties, bioavailability, tolerance, effectiveness, and adverse effects. Therapies with hyaluronic acid provided long-lasting, pain relieving, moisturizing, lubricating, and dermal filling effect. Tissue hydration, elasticity, and durability improved. Adjunct therapy with hyaluronic acid provides longer-lasting therapeutic effect when compared to the use of glucocorticosteroids and NSAIDs in osteoarthritic chronic diseases, is well-established in ophthalmology due to its lubricating properties for the corneal endothelium, and improves tissue hydration and cellular resistance to mechanical damage in aesthetic dermatology, and has marginal adverse effects. Several trials indicated its role in tumor markers, liver diseases, and in pharmaceuticals, but further research would be necessary to draw conclusive results in those fields.
Author Wcisło-Dziadecka, Dominika L
Salwowska, Natalia M
Bebenek, Katarzyna A
Żądło, Dominika A
Author_xml – sequence: 1
  givenname: Natalia M
  surname: Salwowska
  fullname: Salwowska, Natalia M
  organization: Department of Dermatology, Andrzej Mielęcki Memorial Independent Public Clinical Hospital in Katowice, Katowice, Poland
– sequence: 2
  givenname: Katarzyna A
  surname: Bebenek
  fullname: Bebenek, Katarzyna A
  organization: Department of Medicine, Adventist Hinsdale Hospital, IL, Hinsdale, USA
– sequence: 3
  givenname: Dominika A
  surname: Żądło
  fullname: Żądło, Dominika A
  organization: Department of General and Endocrine Surgery, School of Medicine in Bytom Division of Dentistry in Zabrze, Medical University of Silesia, Katowice, Poland
– sequence: 4
  givenname: Dominika L
  surname: Wcisło-Dziadecka
  fullname: Wcisło-Dziadecka, Dominika L
  email: ddziadecka@interia.pl, ddziadecka@interia.pl
  organization: Department of Skin Structural Studies, Chair of Cosmetology, School of Pharmacy with Division of Medicine in Sosnowiec, Medical University of Silesia, Sosnowiec, Poland
BackLink https://www.ncbi.nlm.nih.gov/pubmed/27324942$$D View this record in MEDLINE/PubMed
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Issue 4
Keywords adjuvant therapy
long-lasting effect
wound healing
bioavailability
tolerability
hyaluronic acid
Language English
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2016 Wiley Periodicals, Inc.
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PublicationTitle Journal of cosmetic dermatology
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References Toole BP. Hyaluronan: from the extracellular glue that pericellular cue. Nat Rev Cancer 2004; 4: 528-39.
Kultti A, Xiaoming L, Ping J et al. Therapeutic targeting of hyaluronan in the tumor stroma. Cancers 2012; 4: 873-903.
Stern R, Asari AA, Sugahara SC. Hyaluronan fragments: an information-rich system. Eur J Cell Biol 2006; 85: 699-715.
Juhlin L. Hyaluronan in skin. J Intern Med 1997; 242: 61-6.
Maxwell C, McCarthy J, Turley E. Cell-surface and mitotic spindle RHAMM: moonlighting or dual oncogenic functions? J Cell Sci 2008; 121: 925-32.
Jacobetz MA, Chan DS, Neesse A et al. Hyaluronan impairs vascular function and drug delivery in a mouse model of pancreatic cancer. Gut 2013; 62: 112-20.
Moore AR, Willoughby DA. Hyaluronan as a drug delivery system for diclofenac: a hypothesis for the mode of action. Int J Tissue React 1995; 17: 153-6.
Jiang P, Li X, Thompson CB et al. Effective targeting of the tumor microenvironment for cancer therapy. Anticancer Res 2012; 32: 1203-12.
Lepperdinger G, Strobl B, Kreil G. HYAL2, and the human gene Expressed in many cells, encodes a lysosomal Hyaluronidase with a novel type of specificity. J Biol Chem 1998; 273: 22466-70.
Hardwick C, Hoare K, Owens R et al. Molecular cloning of a novel hyaluronan receptor mediates tumor cell that motility. J Cell Biol 1992; 117: 1343-50.
Saari H, Konttinen YT. Determination of synovial fluid hyaluronate concentration and polymerisation by high performance liquid chromatography. Ann Rheum Dis 1989; 48: 565-70.
Volpi N, Schiller J, Stern R et al. Role, metabolism, chemical modifications and applications of hyaluronan. Curr Med Chem 2009; 16: 1718-45.
Lokeshwar VB, Cerwinka WH, Isoyama T et al. HYAL1 hyaluronidase in prostate cancer: a tumor promoter and suppressor. Cancer Res 2005; 65: 7782-9.
Kanchwala SK, Holloway L, Bucky LP. Reliable soft tissue augmentation: a clinical comparison of injectable soft-tissue fillers for facial-volume augmentation. Ann Plast Surg 2005; 55: 30-5.
Schiavinato A, Lini E, Guidolin D et al. Intraarticular sodium hyaluronate injections in the Pond-Nuki experimental model of osteoarthritis in dogs. II. Morphological findings. Clin Orthop Relat Res 1989; 241: 286-99.
Kogan G, Soltes L, Stern R et al. Hyaluronic acid: a natural biopolymer with a broad range of biomedical and industrial applications. Biotechnol Lett 2007; 29: 17-25.
van Beek M, Weeks A, Jones L et al. Immobilized hyaluronic acid containing model silicone hydrogels reduce protein adsorption. J Biomater Sci Polym Ed 2008; 19: 1425-36.
Prehm P. Release of hyaluronate from eukaryotic cells. Biochem J 1990; 267: 185-9.
Moreland LW. Intra-articular hyaluronan (hyaluronic acid) and hylans for the treatment of osteoarthritis: mechanisms of action. Arthritis Res Ther 2003; 5: 54-67.
Szabó A, Zelkó R, Antal I. Treatment of rheumatic diseases with intraarticular drug delivery systems. Acta Pharm Hung 2011; 81: 77-86.
Lathrop WF, Carmichael EP, Myles DG et al. cDNA cloning reveals the molecular structure of a sperm surface protein PH-20, involved in sperm-egg adhesion and the wide distribution of its gene among mammals. J Cell Biol 1990; 111: 2939-49.
Tezel A, Fredrickson GH. The science of hyaluronic acid dermal fillers. J Cosmet Laser Ther 2008; 10: 35-42.
Hamerman D, Schuster H. Hyaluronate in normal human synovial fluid. J Clin Invest 1958; 37: 57-64.
Barbucci R, Lamponi S, Borzacchiello A et al. Hyaluronic acid hydrogel in the treatment of osteoarthritis. Biomaterials 2002; 23: 4503-13.
Ghosh P, Holbert C, Read R et al. Hyaluronic acid (hyaluronan) in experimental osteoarthritis. J Rheumatol Suppl 1995; 43: 155-7.
Bates EJ, Harper GS, Lowther DA et al. Effect of oxygen-derived reactive species on cartilage proteoglycan-hyaluronate aggregates. Biochem Int 1984; 8: 629-37.
Balogh L, Polyak A, Mathe D et al. Absorption, uptake and tissue affinity of high-molecular-weight hyaluronan after oral administration in rats and dogs. J Agric Food Chem 2008; 56: 10582-93.
Meyer F, Palmer JW. The polysaccharide of the vitreous humor. J Biol Chem 1934; 107: 629-34.
Weissmann B, Meyer K. The structure of hyalobiuronic acid and of hyaluronic acid from umbilical cord. J Am Chem Soc 1954; 76: 1753-7.
Koyama H, Hibi T, Isogai Z et al. Hyperproduction of hyaluronan in neu-induced mammary tumor angiogenesis accelerates through stromal cell recruitment: possible involvement of versican/PG-M. Am J Pathol 2007; 170: 1086-99.
Jacobson A, Rahmanian M, Rubin K et al. Expression of hyaluronan synthase 2 or Hyaluronidase 1 differentially: affect the growth rate of colon carcinoma cell transplantable tumors. Int J Cancer 2002; 102: 212-9.
Maclennan AP. The production of capsules, hyaluronic acid and Hyaluronidase to 25 strains of group C streptococci. J Gen Microbiol 1956; 15: 485-91.
Washburn NR, Prata JE, Friedrich EE et al. Polymer-conjugated inhibitors of tumor necrosis factor-α for local control of inflammation. Biomatter 2013; 3: e25597.
Andre P. New trends in face rejuvenation by hyaluronic acid injections. J Cosmet Dermatol 2008; 7: 251-8.
Gupta S, Hawker GA, Laporte A et al. The economic burden of disabling hip and knee osteoarthritis (OA) from the perspective of Individuals living with this condition. Rheumatology 2005; 44: 1531-7.
Maltese A, Borzacchiello A, Mayol L et al. Novel polysaccharides-based viscoelastic formulations for ophthalmic surgery: rheological characterization. Biomaterials 2006; 27: 5134-42.
Altman RD, Moskowitz R. Intraarticular sodium hyaluronate (Hyalgan) in the treatment of patients with osteoarthritis of the knee: a randomized clinical trial. Hyalgan Study Group. J Rheumatol 1998; 25: 2203-12.
Slevin M, Krupinski J, Gaffney J et al. Hyaluronan mediated angiogenesis in vascular disease: uncovering RHAMM and CD44 receptor signaling pathways. Matrix Biol 2007; 26: 58-68.
Sugahara SC, Murai T, Nishinakamura H et al. Hyaluronan oligosaccharides induce CD44 cleavage and promote cell migration in CD44-expressing tumor cells. J Biol Chem 2003; 278: 32259-65.
Hemming R, Martin DC, Słomiński E et al. Mouse HYAL3 it encodes a 45-56-kDa glycoprotein overexpression increases whose hyaluronidase 1 activity in cultured cells. Glycobiology 2008; 18: 280-9.
Moskowitz RW. Hyaluronic acid supplementation. Curr Rheumatol Rep 2000; 2: 466-71.
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References_xml – reference: Washburn NR, Prata JE, Friedrich EE et al. Polymer-conjugated inhibitors of tumor necrosis factor-α for local control of inflammation. Biomatter 2013; 3: e25597.
– reference: Andre P. New trends in face rejuvenation by hyaluronic acid injections. J Cosmet Dermatol 2008; 7: 251-8.
– reference: Volpi N, Schiller J, Stern R et al. Role, metabolism, chemical modifications and applications of hyaluronan. Curr Med Chem 2009; 16: 1718-45.
– reference: Moore AR, Willoughby DA. Hyaluronan as a drug delivery system for diclofenac: a hypothesis for the mode of action. Int J Tissue React 1995; 17: 153-6.
– reference: Schiavinato A, Lini E, Guidolin D et al. Intraarticular sodium hyaluronate injections in the Pond-Nuki experimental model of osteoarthritis in dogs. II. Morphological findings. Clin Orthop Relat Res 1989; 241: 286-99.
– reference: Hardwick C, Hoare K, Owens R et al. Molecular cloning of a novel hyaluronan receptor mediates tumor cell that motility. J Cell Biol 1992; 117: 1343-50.
– reference: Maxwell C, McCarthy J, Turley E. Cell-surface and mitotic spindle RHAMM: moonlighting or dual oncogenic functions? J Cell Sci 2008; 121: 925-32.
– reference: Lathrop WF, Carmichael EP, Myles DG et al. cDNA cloning reveals the molecular structure of a sperm surface protein PH-20, involved in sperm-egg adhesion and the wide distribution of its gene among mammals. J Cell Biol 1990; 111: 2939-49.
– reference: Juhlin L. Hyaluronan in skin. J Intern Med 1997; 242: 61-6.
– reference: Jacobetz MA, Chan DS, Neesse A et al. Hyaluronan impairs vascular function and drug delivery in a mouse model of pancreatic cancer. Gut 2013; 62: 112-20.
– reference: Prehm P. Release of hyaluronate from eukaryotic cells. Biochem J 1990; 267: 185-9.
– reference: Szabó A, Zelkó R, Antal I. Treatment of rheumatic diseases with intraarticular drug delivery systems. Acta Pharm Hung 2011; 81: 77-86.
– reference: Kultti A, Xiaoming L, Ping J et al. Therapeutic targeting of hyaluronan in the tumor stroma. Cancers 2012; 4: 873-903.
– reference: Barbucci R, Lamponi S, Borzacchiello A et al. Hyaluronic acid hydrogel in the treatment of osteoarthritis. Biomaterials 2002; 23: 4503-13.
– reference: Moreland LW. Intra-articular hyaluronan (hyaluronic acid) and hylans for the treatment of osteoarthritis: mechanisms of action. Arthritis Res Ther 2003; 5: 54-67.
– reference: Meyer F, Palmer JW. The polysaccharide of the vitreous humor. J Biol Chem 1934; 107: 629-34.
– reference: Toole BP. Hyaluronan: from the extracellular glue that pericellular cue. Nat Rev Cancer 2004; 4: 528-39.
– reference: Altman RD, Moskowitz R. Intraarticular sodium hyaluronate (Hyalgan) in the treatment of patients with osteoarthritis of the knee: a randomized clinical trial. Hyalgan Study Group. J Rheumatol 1998; 25: 2203-12.
– reference: Moskowitz RW. Hyaluronic acid supplementation. Curr Rheumatol Rep 2000; 2: 466-71.
– reference: Maclennan AP. The production of capsules, hyaluronic acid and Hyaluronidase to 25 strains of group C streptococci. J Gen Microbiol 1956; 15: 485-91.
– reference: Ghosh P, Holbert C, Read R et al. Hyaluronic acid (hyaluronan) in experimental osteoarthritis. J Rheumatol Suppl 1995; 43: 155-7.
– reference: Weissmann B, Meyer K. The structure of hyalobiuronic acid and of hyaluronic acid from umbilical cord. J Am Chem Soc 1954; 76: 1753-7.
– reference: Kanchwala SK, Holloway L, Bucky LP. Reliable soft tissue augmentation: a clinical comparison of injectable soft-tissue fillers for facial-volume augmentation. Ann Plast Surg 2005; 55: 30-5.
– reference: Jiang P, Li X, Thompson CB et al. Effective targeting of the tumor microenvironment for cancer therapy. Anticancer Res 2012; 32: 1203-12.
– reference: Tezel A, Fredrickson GH. The science of hyaluronic acid dermal fillers. J Cosmet Laser Ther 2008; 10: 35-42.
– reference: Stern R, Asari AA, Sugahara SC. Hyaluronan fragments: an information-rich system. Eur J Cell Biol 2006; 85: 699-715.
– reference: Hamerman D, Schuster H. Hyaluronate in normal human synovial fluid. J Clin Invest 1958; 37: 57-64.
– reference: Gupta S, Hawker GA, Laporte A et al. The economic burden of disabling hip and knee osteoarthritis (OA) from the perspective of Individuals living with this condition. Rheumatology 2005; 44: 1531-7.
– reference: Kogan G, Soltes L, Stern R et al. Hyaluronic acid: a natural biopolymer with a broad range of biomedical and industrial applications. Biotechnol Lett 2007; 29: 17-25.
– reference: Hemming R, Martin DC, Słomiński E et al. Mouse HYAL3 it encodes a 45-56-kDa glycoprotein overexpression increases whose hyaluronidase 1 activity in cultured cells. Glycobiology 2008; 18: 280-9.
– reference: Lokeshwar VB, Cerwinka WH, Isoyama T et al. HYAL1 hyaluronidase in prostate cancer: a tumor promoter and suppressor. Cancer Res 2005; 65: 7782-9.
– reference: Sugahara SC, Murai T, Nishinakamura H et al. Hyaluronan oligosaccharides induce CD44 cleavage and promote cell migration in CD44-expressing tumor cells. J Biol Chem 2003; 278: 32259-65.
– reference: Koyama H, Hibi T, Isogai Z et al. Hyperproduction of hyaluronan in neu-induced mammary tumor angiogenesis accelerates through stromal cell recruitment: possible involvement of versican/PG-M. Am J Pathol 2007; 170: 1086-99.
– reference: Maltese A, Borzacchiello A, Mayol L et al. Novel polysaccharides-based viscoelastic formulations for ophthalmic surgery: rheological characterization. Biomaterials 2006; 27: 5134-42.
– reference: Saari H, Konttinen YT. Determination of synovial fluid hyaluronate concentration and polymerisation by high performance liquid chromatography. Ann Rheum Dis 1989; 48: 565-70.
– reference: Slevin M, Krupinski J, Gaffney J et al. Hyaluronan mediated angiogenesis in vascular disease: uncovering RHAMM and CD44 receptor signaling pathways. Matrix Biol 2007; 26: 58-68.
– reference: Balogh L, Polyak A, Mathe D et al. Absorption, uptake and tissue affinity of high-molecular-weight hyaluronan after oral administration in rats and dogs. J Agric Food Chem 2008; 56: 10582-93.
– reference: van Beek M, Weeks A, Jones L et al. Immobilized hyaluronic acid containing model silicone hydrogels reduce protein adsorption. J Biomater Sci Polym Ed 2008; 19: 1425-36.
– reference: Lepperdinger G, Strobl B, Kreil G. HYAL2, and the human gene Expressed in many cells, encodes a lysosomal Hyaluronidase with a novel type of specificity. J Biol Chem 1998; 273: 22466-70.
– reference: Jacobson A, Rahmanian M, Rubin K et al. Expression of hyaluronan synthase 2 or Hyaluronidase 1 differentially: affect the growth rate of colon carcinoma cell transplantable tumors. Int J Cancer 2002; 102: 212-9.
– reference: Bates EJ, Harper GS, Lowther DA et al. Effect of oxygen-derived reactive species on cartilage proteoglycan-hyaluronate aggregates. Biochem Int 1984; 8: 629-37.
– volume: 121
  start-page: 925
  year: 2008
  end-page: 32
  article-title: Cell‐surface and mitotic spindle RHAMM: moonlighting or dual oncogenic functions?
  publication-title: J Cell Sci
– volume: 32
  start-page: 1203
  year: 2012
  end-page: 12
  article-title: Effective targeting of the tumor microenvironment for cancer therapy
  publication-title: Anticancer Res
– volume: 241
  start-page: 286
  year: 1989
  end-page: 99
  article-title: Intraarticular sodium hyaluronate injections in the Pond‐Nuki experimental model of osteoarthritis in dogs. II. Morphological findings
  publication-title: Clin Orthop Relat Res
– volume: 267
  start-page: 185
  year: 1990
  end-page: 9
  article-title: Release of hyaluronate from eukaryotic cells
  publication-title: Biochem J
– volume: 25
  start-page: 2203
  year: 1998
  end-page: 12
  article-title: Intraarticular sodium hyaluronate (Hyalgan) in the treatment of patients with osteoarthritis of the knee: a randomized clinical trial. Hyalgan Study Group
  publication-title: J Rheumatol
– volume: 111
  start-page: 2939
  year: 1990
  end-page: 49
  article-title: cDNA cloning reveals the molecular structure of a sperm surface protein PH‐20, involved in sperm‐egg adhesion and the wide distribution of its gene among mammals
  publication-title: J Cell Biol
– volume: 15
  start-page: 485
  year: 1956
  end-page: 91
  article-title: The production of capsules, hyaluronic acid and Hyaluronidase to 25 strains of group C streptococci
  publication-title: J Gen Microbiol
– volume: 5
  start-page: 54
  year: 2003
  end-page: 67
  article-title: Intra‐articular hyaluronan (hyaluronic acid) and hylans for the treatment of osteoarthritis: mechanisms of action
  publication-title: Arthritis Res Ther
– volume: 16
  start-page: 1718
  year: 2009
  end-page: 45
  article-title: Role, metabolism, chemical modifications and applications of hyaluronan
  publication-title: Curr Med Chem
– volume: 102
  start-page: 212
  year: 2002
  end-page: 9
  article-title: Expression of hyaluronan synthase 2 or Hyaluronidase 1 differentially: affect the growth rate of colon carcinoma cell transplantable tumors
  publication-title: Int J Cancer
– volume: 18
  start-page: 280
  year: 2008
  end-page: 9
  article-title: Mouse HYAL3 it encodes a 45–56‐kDa glycoprotein overexpression increases whose hyaluronidase 1 activity in cultured cells
  publication-title: Glycobiology
– volume: 170
  start-page: 1086
  year: 2007
  end-page: 99
  article-title: Hyperproduction of hyaluronan in neu‐induced mammary tumor angiogenesis accelerates through stromal cell recruitment: possible involvement of versican/PG‐M
  publication-title: Am J Pathol
– volume: 4
  start-page: 873
  year: 2012
  end-page: 903
  article-title: Therapeutic targeting of hyaluronan in the tumor stroma
  publication-title: Cancers
– volume: 85
  start-page: 699
  year: 2006
  end-page: 715
  article-title: Hyaluronan fragments: an information‐rich system
  publication-title: Eur J Cell Biol
– volume: 10
  start-page: 35
  year: 2008
  end-page: 42
  article-title: The science of hyaluronic acid dermal fillers
  publication-title: J Cosmet Laser Ther
– volume: 23
  start-page: 4503
  year: 2002
  end-page: 13
  article-title: Hyaluronic acid hydrogel in the treatment of osteoarthritis
  publication-title: Biomaterials
– volume: 17
  start-page: 153
  year: 1995
  end-page: 6
  article-title: Hyaluronan as a drug delivery system for diclofenac: a hypothesis for the mode of action
  publication-title: Int J Tissue React
– volume: 7
  start-page: 251
  year: 2008
  end-page: 8
  article-title: New trends in face rejuvenation by hyaluronic acid injections
  publication-title: J Cosmet Dermatol
– start-page: 205
  year: 1998
  end-page: 17
– volume: 37
  start-page: 57
  year: 1958
  end-page: 64
  article-title: Hyaluronate in normal human synovial fluid
  publication-title: J Clin Invest
– volume: 278
  start-page: 32259
  year: 2003
  end-page: 65
  article-title: Hyaluronan oligosaccharides induce CD44 cleavage and promote cell migration in CD44‐expressing tumor cells
  publication-title: J Biol Chem
– volume: 3
  start-page: e25597
  year: 2013
  article-title: Polymer‐conjugated inhibitors of tumor necrosis factor‐ for local control of inflammation
  publication-title: Biomatter
– volume: 8
  start-page: 629
  year: 1984
  end-page: 37
  article-title: Effect of oxygen‐derived reactive species on cartilage proteoglycan‐hyaluronate aggregates
  publication-title: Biochem Int
– volume: 2
  start-page: 466
  year: 2000
  end-page: 71
  article-title: Hyaluronic acid supplementation
  publication-title: Curr Rheumatol Rep
– volume: 29
  start-page: 17
  year: 2007
  end-page: 25
  article-title: Hyaluronic acid: a natural biopolymer with a broad range of biomedical and industrial applications
  publication-title: Biotechnol Lett
– volume: 26
  start-page: 58
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Snippet Summary Background Hyaluronic acid is a widely available, biocompatible, polysaccharide with distinguishing physiochemical properties which inspire its...
Hyaluronic acid is a widely available, biocompatible, polysaccharide with distinguishing physiochemical properties which inspire its application throughout...
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SubjectTerms adjuvant therapy
bioavailability
Biological Availability
Cosmetic Techniques
Dermal Fillers - adverse effects
Dermal Fillers - pharmacokinetics
Dermal Fillers - therapeutic use
Dry Eye Syndromes - drug therapy
Humans
hyaluronic acid
Hyaluronic Acid - adverse effects
Hyaluronic Acid - metabolism
Hyaluronic Acid - pharmacokinetics
Hyaluronic Acid - therapeutic use
long-lasting effect
Neoplasms - metabolism
Osteoarthritis - drug therapy
Randomized Controlled Trials as Topic
tolerability
Viscosupplements - adverse effects
Viscosupplements - pharmacokinetics
Viscosupplements - therapeutic use
wound healing
Title Physiochemical properties and application of hyaluronic acid: a systematic review
URI https://api.istex.fr/ark:/67375/WNG-9THWH5X1-7/fulltext.pdf
https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fjocd.12237
https://www.ncbi.nlm.nih.gov/pubmed/27324942
https://www.proquest.com/docview/1826701254
Volume 15
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