치의학 분야에서 히알루론산의 용도는 무엇인가요?
루 론 산, also known as hyaluronan, is an acidic mucopolysaccharide composed 의D-glucuronic 산disaccharide units 그리고N-acetylglucosamine [1]다. It is widely distributed 에서이connective tissue 사이human cells, the vitreous body of the eye, and synovial fluid in the joints. It is an important component of the skin. 루 론acid is a high-molecular polymer with an average molecular weight ranging from 100,000 to 10 milli에daltons (unit of mass). Its molecular structure is shown in Figure 1 [2].
이molecular structure of 루 론acid is surrounded by many functional groups such as hydroxyl and carboxyl groups, making it soluble in water but insoluble in organic solvents such as ethanol and ether. These functional groups make it a very strong water absorbent through hydrogen bonding and other effects. Hyaluronic acid is a white, pasty or fibrous substance with a faint odour. It is a highly absorbent substance that dissolves slowly and completely in water. It can absorb thousands of times its own molecular weight in water, which is much more than other polysaccharide compounds. Therefore, hyaluronic acid is a natural moisturiser in nature [3-4].
The applicati에fields of hyaluronic acid are gradually expanding with further research, including medicine, cosmetics, health food and beauty injections. Despite its superior properties and wide range of applications, hyaluronic acid is limited in its use due to its complex molecular structure, which causes reactions 사이or within molecules, and the addition of hyaluronic acid can easily increase the viscosity and consistency of the system. This article summarises the preparation methods, special properties and influencing factors of hyaluronic acid, and describes the application fields of hyaluronic acid.
히알루론산의 제조 방법 1
세 가지가 있다main methods for preparing hyaluronic acid:동물 추출, 미생물 발효 및 화학 합성 [5-7].동물 추출은 현재 히알루론산을 준비하는 주요 방법이며 일반적으로 사람의 탯줄, 동물의 유리 볼, 닭 빗 또는 고래 연골과 같은 신선한 동물 조직에서 추출할 수 있습니다.그러나 원료의 공급이 제한되어 있어 가격이 비싸다.또한 이러한 원료에 함유된 히알루론산 함량이 낮아 수율이 낮습니다.추출 방법의 복잡성과 더불어 증가하는 연구 및 응용 수요를 충족시킬 수 없습니다.미생물 발효방법에서, 히알루론산은 Streptococcus equi, Streptococcus zooecus, Streptococcus equinus를 발효시켜 제조할 수 있다.이 방법은 동물조직 추출법에 비해 일정한 장점이 있다.
The raw materials for this method are readily available, the sources are relatively abundant, the cost is low, and the extraction process is simple and convenient. However, hyaluronidase is easily produced during the entire preparation process, so the production process needs to be well controlled. The chemical synthesis method is relatively cheaper than the previous two. It mainly synthesises ‘hyaluronic acid oxaziridine derivatives’ through polysaccharide polymers, and then adds a certain amount of decomposing enzyme. The process of precipitation, separation and purification is used to produce synthetic hyaluronic acid, which has successfully replaced natural hyaluronic acid.
히알루론산의 성질과 특성 2
Hyaluronic acid is a high-molecular polymer with active functional groups such as carboxyl groups, hydroxyl groups, N-acetyl groups and reducing ends distributed on the surface. It can not only be modified by cross-linking, esterification, grafting, molecular modification and compounding, but also form hydrogen bonds with water molecules and adsorb a large amount of water. Studies have found that 1 g of hyaluronic acid can adsorb 6 L of water, far exceeding the water adsorption capacity of other substances [8]. Therefore, hyaluronic acid is widely used as a moisturising agent in cosmetic products.
Hyaluronic acid is able to form a network structure in a solvent, changing the rheological properties of the solution. The molecular structure of hyaluronic acid has hydrophilic reactive functional groups on the surface, which spread out in a solvent, occupying a lot of space. As the concentration increases, the interactions between the intra-or intermolecular chains of these macromolecules can form a network structure, which leads to an increase in the viscosity and elasticity of the solution and causes unique rheological properties [9]. Hyaluronic acid molecules have a relatively stable molecular structure, but are sensitive to changes in ionic strength and pH in the solution [10].
Molecular diffusion often occurs in solutions with low ionic strength due to the repulsion between charges, which increases the viscosity of the solution [11]. When dilute solutions expand, hyaluronic acid molecules slowly become longer and wider in the solution, eventually forming a round substance. When the concentration of the solution exceeds 1%, hyaluronic acid can form a continuous network structure. The higher the concentration, the more serious the phenomenon of crossing and overlapping. In addition, the cross-linking and interaction between molecular chains form a double-helix structure, which makes the formed network structure more stable. The more serious the phenomenon is in hyaluronic acid molecules with high molecular weight and large molecular volume [12-13], the greater the change in the physical properties of hyaluronic acid.
Hyaluronic acid is generally used in higher-end products and added in very small amounts. This is partly due to the fact that hyaluronic acid is expensive and its sources are limited, and partly due to the properties it exhibits. Natural hyaluronic acid has a short half-life, is easily degraded and diffused, has poor stability and is overly water-soluble [14]. In addition, the active functional groups within or between hyaluronic acid molecules are prone to react in an electrolyte, causing cross-linking and overlap between the chains of the molecule itself or adjacent molecules to form a mass of material. In addition to strictly limiting the amount of hyaluronic acid added, the experiment also needs to control the dissolution process of hyaluronic acid. Its highly water-absorbent nature makes it very easy to disperse unevenly in many aqueous systems, and also increases the consistency of the system [15], making the system state difficult to control.
히알루론산 적용 3
3. 화장품에 적용 1
Due to its special molecular structure, hyaluronic acid has been widely used in cosmetics as a moisturising agent. Compared with other moisturisers, it has a better moisturising effect and is suitable for the moisturising requirements of cosmetics in different environments and humidity levels [16]. It is also non-greasy and does not block the pores of the skin. Hyaluronic acid itself is a high-molecular polymer with a strong lubricating effect and film-forming properties. Cosmetics containing hyaluronic acid feel noticeably smoother when applied, feel good on the skin and form a thin film on the skin's 표면은 적용 후 피부에 부드러움과 수분의 좋은 느낌을 주고 표피를 보호합니다.
In addition, hyaluronic acid, either alone or in combination with phospholipids, can be added to the aqueous or oily medium to emulsify the cosmetic product. This natural emulsifier is environmentally friendly and safe, and can be used in the production of food, skin creams, lotions, facial cleansers, etc. Hyaluronic acid with a molecular weight of more than 3000KD has good viscosity and can be used as a good thickener in cosmetics. Macromolecular hyaluronic acid not only forms a protective film on the surface of the substrate, but also acts as a molecular capsule to encapsulate small molecules. It is especially suitable for use in some fragrance products, combining with fragrance molecules and encapsulating them, so as to not only slow down the volatilisation of the fragrance and make it last longer, but also prevent the fragrance from coming into direct contact with the skin, causing adverse reactions such as irritation and other allergic symptoms.
In addition, hyaluronic acid itself is a component of skin tissue, regulating the diffusion and transport of proteins, water and electrolytes. Exogenous hyaluronic acid also plays a supplementary role to endogenous hyaluronic acid. Hyaluronic acid with a smaller molecular weight can penetrate into the superficial layer of the skin, supplying the skin with nutrients and excreting waste products, preventing skin ageing, playing a role in beauty and skin care, prolonging the adhesion of make-up and lipstick on the skin, etc., and is a commonly used product in some beauty salons and cosmetics production sites. Loureiro Borghetti et al. [17] studied the effect of hyaluronic acid on the mouse mouth from a clinical and histological perspective, and found that a hyaluronic acid solution at a certain concentration can stimulate collagen formation. Some scholars have found that hyaluronic acid is beneficial to tissue repair and slightly protects collagen formation. Adding a certain amount of hyaluronic acid to hair care products can also have the effect of smoothing the hair. The above shows that hyaluronic acid is a good cosmetic ingredient.
3. 2의학에의 응용
Hyaluronic acid is used in ophthalmology, rhinology, laryngology, orthopaedics and general surgery. Hyaluronic acid 젤is used as a filling agent in ophthalmological operations such as extracapsular cataract extraction, intraocular lens implantation, retinal detachment and corneal transplantation. A dilute solution of hyaluronic acid is also used to treat dry keratoconjunctivitis syndrome. Hyaluronic acid's 적출 및 완충 효과는 골관절염, 오십견 및 류마티스 관절염 등 증상을 치료하는 데 사용할 수 있습니다.그것은 또한 간질 방광염을 치료하고 방광 epithelium&를 보호하기 위해 비뇨기과에서 사용할 수 있습니다#39;s glycosaminoglycan 보호층 [18]..
Because the outer layer of the hyaluronic acid molecule is rich in active functional groups, it can bind to many drug molecules and become a carrier that delivers various drugs to pathological sites, overcoming the problem of drugs being degraded before reaching the pathological site. Before binding to the drug molecule, hyaluronic acid needs to be cross-linked and modified, and the receptor hyaluronic acid needs to be selected to a certain extent, so that the drug can be fully located at the pathological site and slowly released, which can greatly enhance the efficacy of the drug [19]. For example, hyaluronic acid is often used to form a complex with BMP (bone morphogenetic protein), which can be injected into the affected area to slowly release BMP and exert its osteogenic effect.
3. 3 경구분야에 적용
Because hyaluronic acid has antibacterial, anti-inflammatory and anti-edema effects, it has been medically proven that the application of hyaluronic acid 젤can alleviate the symptoms of plaque gingivitis, a common infectious disease of the gingival tissue. Compared with the therapeutic effect of hyaluronic acid alone, the combination of scaling and root planing can more effectively improve the recovery of gingival inflammation and clinical indicators. Hyaluronic acid combined with subgingival scaling and root surface smoothing can quickly reduce the inflammatory response of periodontal tissue in patients with chronic periodontitis [20] (see Figures 3 and 4 below).
Studies have also shown that hyaluronic acid combined with guided periodontal tissue regeneration can promote alveolar bone recovery and bone mineralisation in the treatment of chronic periodontitis. Hyaluronic acid itself is a component of the extracellular matrix of periodontal connective tissue and regulates the hydration of the extracellular matrix. Hyaluronic acid with a relatively high molecular weight can also inhibit the proliferation of gingival epithelial cells, lymphocytes and fibroblasts, shorten the inflammatory process of periodontitis and improve the condition. Domestic and foreign studies have shown that after mechanical treatment of periodontitis patients or after periodontal surgery, hyaluronic acid gel can reduce periodontal tissue destruction, alleviate periodontal inflammation and promote the recovery of periodontal tissue.
Zhang Li et al. [22] found that hyaluronic acid can significantly reduce the peri-implant sulcus bleeding index and plaque index in patients with peri-implant mucositis, and is more effective than mechanical plaque and calculus removal. At the same time, some researchers have found that after mechanical plaque removal and SRP, injecting a mixed solution of a certain proportion of chlorhexidine and hyaluronic acid into the periodontal pocket significantly improves the peri-implant index, indicating that hyaluronic acid combined with chlorhexidine has a good effect on the treatment of peri-implantitis.
In addition to studies that have proven its ability to kill bacteria and prevent the formation of plaque, hyaluronic acid also has certain applications in the healing of tooth extraction wounds. Mendes et al. [23] injected relatively large molecule hyaluronic acid gel into the tooth extraction wounds of rats, and observed and analysed the tissue and morphology of the wound healing process at irregular intervals. They found that after 21 days, the amount of bone formation at the extraction site had increased, and the deposition of bone matrix and cell arrangement were more orderly. Some researchers [24] also conducted experiments on rabbits, injecting 0.8% hyaluronic acid gel into their tooth extraction sockets.
After a period of time, it was found that a large amount of alveolar bone had formed in the extraction sockets. Zeng Yunting and others analysed that this is because hyaluronidase in the extraction wound can break down hyaluronic acid with a relatively large molecular weight into small molecular hyaluronic acid to stimulate osteogenic inductive factors and promote wound healing. Lai Hanbiao et al. [25] confirmed that hyaluronic acid gel and physiological saline were used to treat 50 patients after dental implant surgery, and found that hyaluronic acid gel can significantly promote wound healing, improve redness and swelling, and reduce patient pain.
놀란 등 [26]이 사용했다0.2% hyaluronic acid gel by mass fraction to treat 되풀이 되는aphthousulcers, found that it could immediately relieve symptoms and promote ulcer healing. Lee et al. [27] also studied the efficacy and safety of hyaluronic acid in the treatment of 되풀이 되는aphthous ulcers and conducted a large number of clinical trials. They found that after two weeks, most patients experienced improved pain after using hyaluronic acid, nearly half of them had a reduction in the number of ulcers, and the ulcer area decreased in about 78% of patients. All of the above strongly proves that hyaluronic acid can protect the 경구mucosa, resist inflammation and edema, and effectively improve various oral wounds and inflammations.
4 요약
Hyaluronic acid is a high-molecular polysaccharide substance with a unique molecular structure that is both hydrophilic and hydrophobic. It can undergo various chemical modifications through esterification, amidation and reductive amination reactions. This environmentally friendly and safe compound has broad application prospects. First, hyaluronic acid itself has good water absorption and moisturising properties, and it is also a component of skin tissue. It can supplement the lack of endogenous hyaluronic acid, and can be used as a moisturising agent in cosmetics as well as having an anti-ageing effect. Hyaluronic acid also has antiseptic, anti-inflammatory and anti-edema effects. It can be used alone or in combination with other drugs or surgical treatments to improve symptoms such as gingivitis, periodontitis, mucositis around dental implants, wounds from tooth extraction and 되풀이 되는aphthous ulcers. As hyaluronic acid production technology improves, its use in cosmetics, pharmaceuticals and dentistry will continue to be promoted.
참조
[1] 왕장링 (Wang Jiangling), 런웨이즈 (Ran Weizhi)[식품영양학] 히알루론산과 그 유도체의 현황 및 개발동향 [J.헤이룽장의학, 2014, 37 (6), 117-118
[2] 릴리 안 C. 베 커, 윌 마 F. Bergfeld, 도널드 V. 벨시토, 커티스 D. Klaasen, 제임스 G. 마크 주니어, 로널드 C. 생 크, 토마스 J. Slaga, 폴 W. 스나이더, 화장품 성분 검토 전문가 패널, 그리고 F. 앨런 앤더슨. 히알루로닉의 안전성 평가 최종 보고서 산성, 칼륨, Hyaluronate, 그리고 나트륨 Hyaluronate, 국제 독성학 저널. Vol. 28일, 아니. 2009년 7월/8월 4S
[3] 우동루, ed. Biochemistry of Sugars.북경:고등교육출판사, 1987:627
[4] 성우는 나가이 마사요시.화장품 재료다.JP Show 62-158203, 1987년
[5] 천종지, 구아일.히알루론산 [J]의 응용 및 생산.허난 화학 산업, 2007, 24, 48-49
[6] 팔미에리 B, 메리기 A, 코르바시오 D 등. 고정 조합 히알루론산과 콘드로이틴의 -증상 치료를 위한 무작위 이중 맹검, 위약 대조 연구에서 황산 경구 제형 비침식성 위식도 역류 환자에서 [J. Eur Rev 메드 Pharmacol Sci,2011,17 (24):3272-3278
[7] 저우판구, 마베이레이, 치우보 외.히알루론산/키토산 미립구가 염증성 조골세포에서 matrix metalloproteinase의 발현과 저해인자 mRNA에 미치는 영향 (J.중국실험외과학회지, 2013, 30(11):2377-2379
[8] 빌렉 G, 빌렉 D. 히알루론산 (Hyaluronic acid:the history of an active in-gredient in cosmetics) [독일어][J]. Parfuem Kosmet다. 1988년;69:788개 - 790;792-795
[9]Laurent TC, 히알루론산의 구조. 뉴욕,NY:Ac-ademic Press;1970
[10]Cleland RL,Wang JL,Detweiler DM,Polyelectrolyte proper-sodium hyaluronate의 연결. 2:히알루론산의 전위차 적정. 거대분자 J다 [J다] 1982년;15:386-395
[11] 발라즈 에아, 로랑 TC. 고분자 전해질로서 히알루론산의 점도기능 [J. J Polym Sci입니다. 1951년;6:665-667
[12] 스캇제, 커밍스 C, 브라스 A, 첸 Y. 수용액 중의 히알루로난의 2차 및 3차 구조, rotary shadowing-electron으로 조사 현미경 and 컴퓨터 시뮬레이션 한다. 생화학 J다 [J다]1991년;274:699-705 쪽
[13] 릴리 안 C. 베 커, 윌 마 F. Berfeld, 도널드 V. 벨시토, 커티스 D. Klaassen, 제임스 G. 마크 주니어, 로널드 C. 생 크, 토마스 J. Slaga, 폴 W. 스나이더, 화장품 성분 검토 전문가 패널, 그리고 F. 앨런 앤더슨. 히알루로닉의 안전성 평가 최종 보고서 산, 히알루론산 칼륨, 히알루론산 나트륨 [J. Internation-al Journal of Taxicology/Vol. 28,No. 2009년 7월/8월 4S
[14] 발라즈 에아, 밴드 P. Hyaluronic 산성:그 구조와 용도.화장품 & 세면용품 [J. 1984년;99:65~72
[15] 스 콧 저다. queous solution에서 히알루로난의 2차 및 3차 구조:일부 생물학적 결과. 1988. 사용 가능 한 at:ht-tp://www.glucoforum다. 괜찮아. Jp/과학/ hyaluronan / HA02/HA02E를 사용한다. html. Accessed 2005년 2월 21일
[16] 루지화수홍 Xu Hong, Lu Zhihua.화장품에서의 히알루론산나트륨 적용 [J.중국생약학회지, 1998, 19(5), 222-223.
[17] 루키엘리 루레이로 보르게티, 카를론 프로스 데 바르가스, 사브리나 포자티 모우, 페르난다 곤칼베스 살룸, 마리아 안토니아 잔카나로 데 Figueiredo, 포 르 투 알레. rat tongue[J],ORAL and MAXILLOFACIAL SUR-GERY,2012,113 (4),499-494
[18] 리연윤, fayong.치의학 분야에서 히알루론산의 응용에 대한 진행.국제치과학회지, 2013, 40(3), 344-346.
[19]Lee JH,Jung JY,Bang D. 국소의 효능 0.2% 하이랄-우론산 gel on 되풀이 되는 oral 궤양: 비교 between 되풀이 되는 아프타성 궤양과 베체트병의 구강 궤양. J Eur 아카드 Dermatol Venereol,2008,22(5):590-595
[20] 우야페이, 황자오, 쑤이 외.치석치은염 치료에 있어서 Gengigel gel의 효과 (The effect of Gengigel gel in The treatment of plaque gingivitis)실천기공학회지 2005, 21 (4), 540-542
Yiyao.com다.이탈리아 충치치료 히알루론산 계열 (HA) [EB/OL].(2013-6-25) [2015-9-11]이다.http://www.eyar.com/html/new/2013/0625/1717.html
[21] 장리, 천강, 마리안 외.임상연구:임플란트 근점막염 치료를 위한 sodium hyaluronate 투여에 관한 연구 (J.Chinese Journal of 경구Implantology, 2005, 1, 22-24
[22]Mendes RM,Silva GA,Lima MF 외. 나트륨 hyaluromate 쥐의 치아 구멍에서 치유 과정을 가속화한다 [J]. Arch Oral bi-ol,2008,53 (12):1155-1162
[23]Fawzy El-Sayed KM,Dahaba MA,Aboul-Ela S 등. 치주수술과 함께 hyaluroman gel의 lo-cal 적용: 무작위 대조군 재판 [J]이다. Clin Oral 2012년 Investig, 16 (4): 1229-1236
[24] 라이한뱌오, 류이.이식 후 상처 치유에서 히알루론산 젤의 역할 [J.광동치과질병예방관리, 2008, 16(Suppl.):637-638
[25] 놀란 A, 베일리 C, 배드민턴 J 외. 토피의 효능-cal hyaluronic acid in the 관리 of recurrent aphthous 궤양 [J]다. J Oral Pathol Med,2006,35 (8):461-465
[26]Lee JH,Jung JY,Bang D. 국소의 효능 0.2% 하이랄-우론산 gel on recurrent oral 궤양: 비교 between recurrent 아프타성 궤양과 베체트병의 구강 궤양. J Eur 아카드 Dermatol Venereol,2008,22(5):590-595