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Journal articles on the topic 'Sucrose octasulfate'

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1

Lobmann, Ralf, Arthur Grünerbel, Holger Lawall, et al. "Impact of wound duration on diabetic foot ulcer healing: evaluation of a new sucrose octasulfate wound dressing." Journal of Wound Care 29, no. 10 (2020): 543–51. http://dx.doi.org/10.12968/jowc.2020.29.10.543.

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Objective: A common and frequent complication of diabetes is diabetic foot ulcers (DFU), which can have high treatment costs and severe adverse events. This study aims to evaluate the effects of wound duration on wound healing and the impact on costs, including treatment with a new sucrose octasulfate dressing compared with a control dressing. Method: Based on the Explorer study (a two-armed randomised double-blind clinical trial), a cost-effectiveness analysis compared four different patient groups distinguished by their wound duration and additionally two DFU treatment options: a sucrose oct
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2

Desai, Bijoy J., Rio S. Boothello, Akul Y. Mehta, J. Neel Scarsdale, H. Tonie Wright, and Umesh R. Desai. "Interaction of Thrombin with Sucrose Octasulfate." Biochemistry 50, no. 32 (2011): 6973–82. http://dx.doi.org/10.1021/bi2004526.

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3

Lucey, Michael R., Jung Park, John DelValle, Li Dong Wang, and Tadataka Yamada. "Sucrose octasulfate stimulates gastric somatostatin release." American Journal of Medicine 91, no. 2 (1991): S52—S57. http://dx.doi.org/10.1016/0002-9343(91)90451-3.

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4

Rao, Niranjan, Paul W. Brown, Jim Chang, Thomas N. Thompson, Julie Geary, and Kenneth W. Otis. "Mass balance of14C-bismuth sucrose octasulfate in Sprague-Dawley rats: evidence for dissociation of bismuth from sucrose octasulfate." Biopharmaceutics & Drug Disposition 18, no. 9 (1997): 743–51. http://dx.doi.org/10.1002/(sici)1099-081x(199712)18:9<743::aid-bdd62>3.0.co;2-q.

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5

Kulahin, N., V. Kiselyov, A. Kochoyan, et al. "Dimerization effect of sucrose octasulfate on rat FGF1." Acta Crystallographica Section F Structural Biology and Crystallization Communications 64, no. 6 (2008): 448–52. http://dx.doi.org/10.1107/s174430910801066x.

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6

Unwin, Steven E., Timothy A. Weyrauch, and Carole L. Smith. "Primary Skin Irritation Study on Bismuth Sucrose Octasulfate in Rabbits." Journal of the American College of Toxicology 11, no. 6 (1992): 721. http://dx.doi.org/10.3109/10915819209142114.

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7

Sarilla, Suryakala, Sally Y. Habib, Dmitri V. Kravtsov, Anton Matafonov, David Gailani, and Ingrid M. Verhamme. "Sucrose Octasulfate Selectively Accelerates Thrombin Inactivation by Heparin Cofactor II." Journal of Biological Chemistry 285, no. 11 (2010): 8278–89. http://dx.doi.org/10.1074/jbc.m109.005967.

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8

Fannon, Michael, Kimberly Forsten-Williams, Bing Zhao, et al. "Facilitated diffusion of VEGF165 through descemet's membrane with sucrose octasulfate." Journal of Cellular Physiology 227, no. 11 (2012): 3693–700. http://dx.doi.org/10.1002/jcp.24077.

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9

Yeh, Brian K., Anna V. Eliseenkova, Alexander N. Plotnikov, et al. "Structural Basis for Activation of Fibroblast Growth Factor Signaling by Sucrose Octasulfate." Molecular and Cellular Biology 22, no. 20 (2002): 7184–92. http://dx.doi.org/10.1128/mcb.22.20.7184-7192.2002.

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ABSTRACT Sucrose octasulfate (SOS) is believed to stimulate fibroblast growth factor (FGF) signaling by binding and stabilizing FGFs. In this report, we show that SOS induces FGF-dependent dimerization of FGF receptors (FGFRs). The crystal structure of the dimeric FGF2-FGFR1-SOS complex at 2.6-Å resolution reveals a symmetric assemblage of two 1:1:1 FGF2-FGFR1-SOS ternary complexes. Within each ternary complex SOS binds to FGF and FGFR and thereby increases FGF-FGFR affinity. SOS also interacts with the adjoining FGFR and thereby promotes protein-protein interactions that stabilize dimerizati
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10

Desai, Umesh R., Ioncho R. Vlahov, Azra Pervin, and Robert J. Linhardt. "Conformational analysis of sucrose octasulfate by high resolution nuclear magnetic resonance spectroscopy." Carbohydrate Research 275, no. 2 (1995): 391–401. http://dx.doi.org/10.1016/0008-6215(95)00159-q.

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11

Volkin, David B., Adeline M. Verticelli, Kimberly E. Marfia, Carl J. Burke, Henryk Mach, and C. Russell Middaugh. "Sucralfate and soluble sucrose octasulfate bind and stabilize acidic fibroblast growth factor." Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology 1203, no. 1 (1993): 18–26. http://dx.doi.org/10.1016/0167-4838(93)90031-l.

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12

Orlando, R. C., and N. A. Tobey. "Why Does Sucralfate Improve Healing in Reflux Esophagitis?: The Role of Sucrose Octasulfate." Scandinavian Journal of Gastroenterology 25, sup173 (1990): 17–21. http://dx.doi.org/10.3109/00365529009091919.

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13

Wolff, Jeremy J., Tatiana N. Laremore, Franklin E. Leach, Robert J. Linhardt, and I. Jonathan Amster. "Electron Capture Dissociation, Electron Detachment Dissociation and Infrared Multiphoton Dissociation of Sucrose Octasulfate." European Journal of Mass Spectrometry 15, no. 2 (2009): 275–81. http://dx.doi.org/10.1255/ejms.951.

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The structural analysis of sulfated carbohydrates such as glycosaminoglycans (GAGs) has been a long-standing challenge for the field of mass spectrometry. The dissociation of sulfated carbohydrates by collisionally-activated dissociation (CAD) or infrared multiphoton dissociation (IRMPD), which activate ions via vibrational excitation, typically result in few cleavages and abundant SO3 loss for highly sulfated GAGs such as heparin and heparan sulfate, hampering efforts to determine sites of modification. The recent application of electron activation techniques, specifically electron capture di
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14

Arakawa, Tsutomu, Jie Wen, and John S. Philo. "Densimetric determination of equilibrium binding of sucrose octasulfate with basic fibroblast growth factor." Journal of Protein Chemistry 12, no. 6 (1993): 689–93. http://dx.doi.org/10.1007/bf01024927.

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15

Gunay, Nur Sibel, Keiko Tadano-Aritomi, Toshihiko Toida, Ineo Ishizuka, and Robert J. Linhardt. "Evaluation of Counterions for Electrospray Ionization Mass Spectral Analysis of A Highly Sulfated Carbohydrate, Sucrose Octasulfate." Analytical Chemistry 75, no. 13 (2003): 3226–31. http://dx.doi.org/10.1021/ac034053l.

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16

Lobmann, Ralf, Matthias Augustin, Holger Lawall, et al. "Cost-effectiveness of TLC-sucrose octasulfate versus control dressings in the treatment of diabetic foot ulcers." Journal of Wound Care 28, no. 12 (2019): 808–16. http://dx.doi.org/10.12968/jowc.2019.28.12.808.

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Objective: Diabetes is one of the most widespread diseases in Germany. Common complications are diabetic foot ulcers (DFU), which are associated with a cost-intensive treatment and serious adverse events, such as infections, amputations. This cost-effectiveness analysis compares two treatment options for patients with DFU: a TLC-NOSF dressing versus a neutral dressing, assessed through a European double-blind randomised controlled trial (RCT), Explorer. Methods: The evaluation of the clinical outcomes was associated to direct costs (costs for dressings, nursing time, hospitalisation etc.) of b
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17

Shen, Jun, and Laura E. Lerner. "A comparison of the conformation of sucrose octasulfate, free and bound to acidic fibroblast growth factor." Carbohydrate Research 273, no. 2 (1995): 115–27. http://dx.doi.org/10.1016/0008-6215(95)00062-x.

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18

Nair, Harikrishna, N. Venkateshwaran, Selva Seetharaman S, Wuquan Deng, Apinan Uthaipaisanwong, and Emilio Galea. "Benefits of sucrose octasulfate (TLC-NOSF) dressings in the treatment of chronic wounds: a systematic review." Journal of Wound Care 30, Sup4 (2021): S42—S52. http://dx.doi.org/10.12968/jowc.2021.30.sup4.s42.

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Objective: Management of chronic wounds remains one of the major challenges for health professionals and patients. An evidence-based decision is important to ensure that patients are receiving the best treatment proven to reduce healing time and improve outcomes, including economic benefits and patients' health-related quality of life (HRQoL). Due to recent restrictions because of the COVID-19 pandemic, including closure of wound care centres within hospitals and a drop in patient volume, chronic wound management needs simple-to-use dressings which are still effective and evidence-based soluti
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19

Fannon, Michael, Kimberly Forsten-Williams, Matthew A. Nugent, et al. "Sucrose octasulfate regulates fibroblast growth factor-2 binding, transport, and activity: Potential for regulation of tumor growth." Journal of Cellular Physiology 215, no. 2 (2008): 434–41. http://dx.doi.org/10.1002/jcp.21327.

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20

Zhu, Xiaotian, Barbara T. Hsu, and Douglas C. Rees. "Structural studies of the binding of the anti-ulcer drug sucrose octasulfate to acidic fibroblast growth factor." Structure 1, no. 1 (1993): 27–34. http://dx.doi.org/10.1016/0969-2126(93)90006-3.

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21

Goetz, Regina, Andrew Beenken, Omar A. Ibrahimi, et al. "Molecular Insights into the Klotho-Dependent, Endocrine Mode of Action of Fibroblast Growth Factor 19 Subfamily Members." Molecular and Cellular Biology 27, no. 9 (2007): 3417–28. http://dx.doi.org/10.1128/mcb.02249-06.

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ABSTRACT Unique among fibroblast growth factors (FGFs), FGF19, -21, and -23 act in an endocrine fashion to regulate energy, bile acid, glucose, lipid, phosphate, and vitamin D homeostasis. These FGFs require the presence of Klotho/βKlotho in their target tissues. Here, we present the crystal structures of FGF19 alone and FGF23 in complex with sucrose octasulfate, a disaccharide chemically related to heparin. The conformation of the heparin-binding region between β strands 10 and 12 in FGF19 and FGF23 diverges completely from the common conformation adopted by paracrine-acting FGFs. A cleft bet
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22

Prosser, Beverly E., Steven Johnson, Pietro Roversi, et al. "Expression, purification, cocrystallization and preliminary crystallographic analysis of sucrose octasulfate/human complement regulator factor H SCRs 6–8." Acta Crystallographica Section F Structural Biology and Crystallization Communications 63, no. 6 (2007): 480–83. http://dx.doi.org/10.1107/s1744309107020052.

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23

Rashid, Mohammad Abdur, Sadanori Akita, Mohammed Shawkat Razzaque, et al. "Coadministration of Basic Fibroblast Growth Factor and Sucrose Octasulfate (Sucralfate) Facilitates the Rat Dorsal Flap Survival and Viability." Plastic and Reconstructive Surgery 103, no. 3 (1999): 941–48. http://dx.doi.org/10.1097/00006534-199903000-00026.

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24

Baker, Randall J. "Mass spectrometry of basic aluminum sucrose octasulfate using fast atom bombardment with a saturated tetramethylammonium ion sample matrix." Organic Mass Spectrometry 24, no. 10 (1989): 895–97. http://dx.doi.org/10.1002/oms.1210241008.

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25

Silvey, Gary L. "Two‐dimensional and deuterium‐induced, differential‐isotope‐shift nuclear magnetic resonance characterization of potassium sucrose octasulfate and sucralfate." Journal of Pharmaceutical Sciences 81, no. 5 (1992): 471–74. http://dx.doi.org/10.1002/jps.2600810517.

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26

Xue, Yi, Sangwon Lee, Yongcheng Wang, and Ya Ha. "Crystal structure of the E2 domain of amyloid precursor protein-like protein 1 in complex with sucrose octasulfate." Journal of Biological Chemistry 288, no. 48 (2013): 34756. http://dx.doi.org/10.1074/jbc.a111.219659.

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27

Xue, Yi, Sangwon Lee, Yongcheng Wang, and Ya Ha. "Crystal Structure of the E2 Domain of Amyloid Precursor Protein-like Protein 1 in Complex with Sucrose Octasulfate." Journal of Biological Chemistry 286, no. 34 (2011): 29748–57. http://dx.doi.org/10.1074/jbc.m111.219659.

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28

Mlcoch, T., J. Bartakova, K. Chadimova, E. Ornstová, B. Hajickova, and T. Dolezal. "PMD22 COST-EFFECTIVENESS ANALYSIS OF SUCROSE OCTASULFATE (URGOSTART) DRESSING IN THE TREATMENT OF DIABETIC FOOT AND VENOUS LEG ULCERS." Value in Health 22 (November 2019): S673. http://dx.doi.org/10.1016/j.jval.2019.09.1435.

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29

Ke, Yuyong, Steve Lianghong Li, Linda Dongxia Chang, and Theo Kapanadze. "A novel ultra performance liquid chromatography–tandem mass spectrometry method for the determination of sucrose octasulfate in dog plasma." Journal of Chromatography B 978-979 (January 2015): 151–56. http://dx.doi.org/10.1016/j.jchromb.2014.11.031.

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30

Mai, Trọng Trí, та Quang Nam Trần. "Tính hiệu quả và an toàn của gạc sucrose octasulfate trên vết loét bàn chân đái tháo đường: kết quả từ một nghiên cứu quan sát, nhãn mở, đa trung tâm tại Việt Nam". Vietnam Journal of Diabetes and Endocrinology, № 45 (29 квітня 2021): 38–44. http://dx.doi.org/10.47122/vjde.2020.45.6.

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Đặt vấn đề: Dạng muối kali của sucrose octasulfate cho thấy khả năng ức chế các matrix metalloproteinase cũng như tương tác với các yếu tố tăng trưởng làm tăng khả năng lành thương và rút ngắn thời gian điều trị. Mặc dù vậy, chưa có nhiều nghiên cứu về hiệu quả gạc sucrose octasulfate (SO) trên những loại vết loét bàn chân đái tháo đường (VLBCĐTĐ) chỉ do nguyên nhân thần kinh hoặc chưa có biến chứng thần kinh hoặc mạch máu trong điều kiện đời thực. Mục tiêu: Đánh giá tính hiệu quả và an toàn của gạc SO trên trên nhiều loại VLBCĐTĐ trong điều kiện thực tế lâm sàng. Phương pháp nghiên cứu: Nghiê
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31

Yang, In Seok, Tae Gyun Kim, Bum Seok Park, et al. "Crystal structures of aprotinin and its complex with sucrose octasulfate reveal multiple modes of interactions with implications for heparin binding." Biochemical and Biophysical Research Communications 397, no. 3 (2010): 429–35. http://dx.doi.org/10.1016/j.bbrc.2010.05.113.

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32

Ottaviano, Giancarlo, Stella Blandamura, Elena Fasanaro, et al. "Silver sucrose octasulfate nasal applications and wound healing after endoscopic sinus surgery: a prospective, randomized, double-blind, placebo-controlled study." American Journal of Otolaryngology 36, no. 5 (2015): 625–31. http://dx.doi.org/10.1016/j.amjoto.2015.02.014.

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33

Liu, Jieru, Dongxu Chi, Siyan Pan, et al. "Effective co-encapsulation of doxorubicin and irinotecan for synergistic therapy using liposomes prepared with triethylammonium sucrose octasulfate as drug trapping agent." International Journal of Pharmaceutics 557 (February 2019): 264–72. http://dx.doi.org/10.1016/j.ijpharm.2018.12.072.

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34

Nagy, Lajos, Romeo E. Morales, Martin Beinborn, Peter Vattay, and Sandor Szabo. "Investigation of gastroprotective compounds at subcellular level in isolated gastric mucosal cells." American Journal of Physiology-Gastrointestinal and Liver Physiology 279, no. 6 (2000): G1201—G1208. http://dx.doi.org/10.1152/ajpgi.2000.279.6.g1201.

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We tested the hypothesis that recognized gastroprotective agents exert direct protection against ethanol-induced injury in isolated rat gastric mucosal cells in vitro. If protection exists, we also wanted to identify subcellular targets in the reversible and/or irreversible stages of cell injury. Ethanol-induced cell injury was quantified by measuring plasma membrane leakage (trypan blue exclusion and lactate dehydrogenase release), mitochondrial integrity (succinic dehydrogenase), and nuclear damage (ethidium bromide-DNA fluorescence). Initial cell viability and responsiveness were estimated
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35

Edmonds, Michael, José Luis Lázaro-Martínez, Jesus Manuel Alfayate-García, et al. "Sucrose octasulfate dressing versus control dressing in patients with neuroischaemic diabetic foot ulcers (Explorer): an international, multicentre, double-blind, randomised, controlled trial." Lancet Diabetes & Endocrinology 6, no. 3 (2018): 186–96. http://dx.doi.org/10.1016/s2213-8587(17)30438-2.

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36

F. Evensen, Kristin Bjordal, Anne-B, Jan. "Effects of Na-sucrose Octasulfate on Skin and Mucosa Reactions During Radiotherapy of Head and Neck Cancers&A Randomized Prospective Study." Acta Oncologica 40, no. 6 (2001): 751–55. http://dx.doi.org/10.1080/02841860152619188.

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37

RAO, NIRANJAN, PAUL W. BROWN, PHYLLIS YERINO, JIM CHANG, and KIN-KAI HWANG. "COMPARATIVE ABSORPTION OF BISMUTH IN SPRAGUE-DAWLEY RATS FOLLOWING ORAL ADMINISTRATION OF PREPARATIONS CONTAINING BISMUTH SUCROSE OCTASULFATE, BISMUTH SUBSALICYLATE, AND BISMUTH SUBCITRATE." Biopharmaceutics & Drug Disposition 18, no. 1 (1997): 1–8. http://dx.doi.org/10.1002/(sici)1099-081x(199701)18:1<1::aid-bdd996>3.0.co;2-0.

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38

Marianelli, Cinzia, Paola Petrucci, Maria Cristina Comelli, and Gabriella Calderini. "Silver Sucrose Octasulfate (IASOS™) as a Valid Active Ingredient into a Novel Vaginal Gel against Human Vaginal Pathogens: In Vitro Antimicrobial Activity Assessment." PLoS ONE 9, no. 6 (2014): e97791. http://dx.doi.org/10.1371/journal.pone.0097791.

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39

Yang, Wenqian, Zimeng Yang, Jingru Fu та ін. "The influence of trapping agents on the antitumor efficacy of irinotecan liposomes: head-to-head comparison of ammonium sulfate, sulfobutylether-β-cyclodextrin and sucrose octasulfate". Biomaterials Science 7, № 1 (2019): 419–28. http://dx.doi.org/10.1039/c8bm01175c.

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40

Dissemond, Joachim, Matthias Augustin, Michael Dietlein, et al. "Sucrose Octasulfat – Evidenz in der Behandlung chronischer Wunden." Der Hautarzt 71, no. 10 (2020): 791–801. http://dx.doi.org/10.1007/s00105-020-04637-9.

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Zusammenfassung Bei Patienten mit chronischen Wunden sollte neben einer ursächlichen Therapie auch immer eine Wundbehandlung erfolgen. Wiederholt wurde in diesem Kontext über die unzureichende Evidenz von Wundheilungsprodukten diskutiert. An dem Beispiel von TLC(„technology lipido-colloid“)-Sucrose Octasulfat wird in der vorliegenden Übersichtsarbeit gezeigt, dass auch in diesem Bereich eine aussagekräftige Datenlage mit guter Evidenz und Vergleichbarkeit vorliegt. Ein therapeutischer Ansatzpunkt, die Wundheilung zu fördern, ist die Hemmung von Matrixmetalloproteinasen beispielsweise durch Suc
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41

Lázaro-Martínez, José Luis, Marta García-Madrid, Josep M. García-Alamino, Serge Bohbot, José Luis García-Klepzig, and Yolanda García-Álvarez. "Increasing Transcutaneous Oxygen Pressure in Patients With Neuroischemic Diabetic Foot Ulcers Treated With a Sucrose Octasulfate Dressing: A Pilot Study." International Journal of Lower Extremity Wounds, August 28, 2020, 153473462095224. http://dx.doi.org/10.1177/1534734620952244.

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Regarding the positive clinical outcomes of sucrose octasulfate impregnated dressing documented in neuroischemic diabetic foot ulcers (DFUs), we aimed to evaluate the microcirculatory status in patients with neuroischemic DFU through the use of sucrose octasulfate dressing. Eleven patients with neuroischemic DFU were included in a prospective pilot study between July 2019 and March 2020. We evaluated the effect in transcutaneous oxygen pressure (TcPO2; mm Hg) values within the use of a sucrose octasulfate dressing in the course of the healing process of neuroischemic DFUs (UrgoStart Contact, L
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42

"Sucrose octasulfate inhibits cell proliferation but stimulates fibroblast migration." Gastroenterology 108, no. 4 (1995): A141. http://dx.doi.org/10.1016/0016-5085(95)23226-5.

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43

Hayakawa, Takuya, Shizuka Kawasaki, Yutaka Hirayama, et al. "A thin layer of sucrose octasulfate protects the oesophageal mucosal epithelium in reflux oesophagitis." Scientific Reports 9, no. 1 (2019). http://dx.doi.org/10.1038/s41598-019-39087-4.

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44

"336. Structures of the Retargeted AAV-DJ Vector in the Presence and Not of Receptor-Analog Sucrose Octasulfate." Molecular Therapy 21 (May 2013): S130. http://dx.doi.org/10.1016/s1525-0016(16)34671-8.

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45

Wen, Jiabi, Xuejing Jin, Fatima Al Sayah, Jeffrey A. Johnson, Mike Paulden, and Arto Ohinmaa. "Economic Evaluation of Sucrose Octasulfate Dressing for the Treatment of Diabetic Foot Ulcers for Type 2 Diabetes Patients." Canadian Journal of Diabetes, July 2021. http://dx.doi.org/10.1016/j.jcjd.2021.07.001.

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46

Passali, Desiderio, Jacopo Cambi, Francesco Maria Passali, and Luisa Bellussi. "Activity of hypertonic solution with Silver and Potassium Sucrose Octasulfate on nasal symptoms in obstructive rhinopathy with and without rhinosinusitis." SpringerPlus 2, no. 1 (2013). http://dx.doi.org/10.1186/2193-1801-2-668.

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