Knowledge (XXG)

Virosome

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of virosomes are the rapid detection and activation of the immune response against the viral glycoproteins, which can result in a decrease of the virosomes. However, glycoproteins can still induce a prophylactic response against the virus, which helps with establishing virosomes as vaccine delivery systems. If the virosome is administered into the bloodstream, the virosome can disintegrate. However, if the virosome can reach the target quickly enough, the drug delivery will still happen. There are some challenges with virosomes, but there are ways in which the virosome can still help activate the immune response.  
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glycoproteins. As a drug or vaccine delivery mechanism they are biologically compatible with many host organisms and are also biodegradable. The use of reconstituted virally derived proteins in the formation of the virosome allows for the utilization of what would otherwise be the immunogenic properties of a live-attenuated virus, but is instead a safely killed virus. A safely killed virus can serve as a promising
77:. Antigens are molecules that triggers an immune response when targeted by a specific antibody that corresponds to the shape of the antigen. Haemagglutinin is a viral glycoprotein that causes red blood cell agglutination. Neuraminidase are enzymes that break glycosidic linkages. The size and surface molecules presented on of the virosome can be modified so that it can target different types of cells. 103: 65:. Glycoproteins are a type of protein that have an oligosaccharide chain bonded to amino acid chains. The different types of glycoproteins on the surface of the virosome increases the specificity of the target cells because the surface glycoproteins help with recognition as well as the attachments of the virosomes to their target cells. In the case of the influenza virosome, the glycoproteins are 20: 169:
The benefits of virosomes are that the specific structure and small size help with the precision of target cells. The phospholipid membrane protects the virosome from adverse reactions in the body and the membrane allows the virosome to be biocompatible and biodegradable in the body. The challenges
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are infectious agents that can replicate in their host organism, however virosomes do not replicate. The properties that virosomes share with viruses are based on their structure; virosomes are essentially safely modified viral envelopes that contain the phospholipid membrane and surface
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Virosomes deliver antigens and therapeutic agents to their targeted cells. Virosomes can act as immunopotentiating agents and as agents of targeted drug delivery. Virosomes as immunopotentiating agents activate
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Bomsel M, Tudor D, Drillet AS, Alfsen A, Ganor Y, Roger MG, Mouz N, Amacker M, Chalifour A, Diomede L, Devillier G, Cong Z, Wei Q, Gao H, Qin C, Yang GB, Zurbriggen R, Lopalco L, Fleury S (25 February 2011).
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membrane. Inside of the virosome, there is a central cavity that holds the therapeutic molecules such as nucleic acids, proteins, and drugs. On the surface of the virosome, there can be different types of
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Huckriede, Anke; Bungener, Laura; Stegmann, Toon; Daemen, Toos; Medema, Jeroen; Palache, Abraham M.; Wilschut, Jan (2005). "The virosome concept for influenza vaccines".
330: 94:. Virosomes are suspended in saline buffers and are administered through respiratory, parenteral, intravenous, oral, intramuscular, and topical routes. 454:
Waelti, Ernst; Wegmann, Nina; Schwaninger, Ruth; Wetterwald, Antionette; Wingenfeld, Carsten; Rothen-Rutishauser, Barbara; Gimmi, Claude D. (2002).
415:"Immunization with HIV-1 gp41 subunit virosomes induces mucosal antibodies protecting nonhuman primates against vaginal SHIV challenges" 315: 48:
because it won't cause infection and the viral structure allows the virosome to recognize specific components of its target cells.
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bilayer membrane. They have a typical mean diameter of 150 nm. Essentially, virosomes represent reconstituted empty
45: 239:"Virosome, a hybrid vehicle for efficient and safe drug delivery and its emerging application in cancer treatment" 455: 87: 508: 467: 436: 394: 311: 299: 293: 268: 260: 210: 426: 386: 303: 250: 200: 139: 91: 237:
Liu, Hanqing; Tu, Zhigang; Feng, Fan; Shi, Haifeng; Chen, Keping; Xu, Ximing (2015-06-01).
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incorporating virus derived proteins to allow the virosomes to fuse with target cells.
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They were used as a drug carrier mechanism for experimental cancer therapies.
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consisting of unilamellar phospholipid membrane (either a mono- or bi-layer)
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Kapoor, D.; Vyas, R. B.; Lad, C.; Patel, M. (2013-09-14).
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Virosomes are vehicles that have a spherical shape with a
287: 114:, virosomes contain functional viral envelope 8: 430: 254: 204: 193:Journal of Drug Delivery and Therapeutics 18: 179: 7: 232: 230: 228: 226: 224: 154:They are also being considered for 106:Components of an influenza virosome 33:drug or vaccine delivery mechanism 16:Drug or vaccine delivery mechanism 14: 341:from the original on 2009-02-06. 1: 391:10.1016/j.vaccine.2005.04.026 432:10.1016/j.immuni.2011.01.015 525: 331:"Hemagglutinin Definition" 295:Encyclopedia of Immunology 134:envelopes, devoid of the 126:(NA) intercalated in the 58:phospholipid mono/bilayer 494:"Virosome based vaccine" 92:humoral immune responses 23:Components of a Virosome 165:Benefits and challenges 150:Non-influenza virosomes 308:10.1006/rwei.1999.0055 286:Sela, Michael (1998), 256:10.1515/acph-2015-0019 206:10.22270/jddt.v3i5.627 107: 24: 489:"What are virosomes?" 298:, Elsevier, pp.  105: 81:Virosome applications 22: 98:Influenza virosomes 52:Virosomes structure 243:Acta Pharmaceutica 158:vaccine research. 118:: influenza virus 108: 25: 357:meshb.nlm.nih.gov 516: 476: 475: 451: 445: 444: 434: 409: 403: 402: 373: 367: 366: 364: 363: 349: 343: 342: 327: 321: 320: 291: 283: 277: 276: 258: 234: 219: 218: 208: 184: 140:genetic material 524: 523: 519: 518: 517: 515: 514: 513: 499: 498: 485: 480: 479: 460:Cancer Research 453: 452: 448: 411: 410: 406: 376: 374: 370: 361: 359: 351: 350: 346: 329: 328: 324: 318: 285: 284: 280: 236: 235: 222: 186: 185: 181: 176: 167: 152: 132:influenza virus 110:In contrast to 100: 83: 54: 17: 12: 11: 5: 522: 520: 512: 511: 501: 500: 497: 496: 491: 484: 483:External links 481: 478: 477: 466:(2): 437–444. 446: 425:(2): 269–280. 404: 368: 353:"MeSH Browser" 344: 322: 316: 278: 249:(2): 105–116. 220: 199:(5): 143–147. 178: 177: 175: 172: 166: 163: 151: 148: 142:of the source 138:including the 99: 96: 82: 79: 71:haemagglutinin 53: 50: 15: 13: 10: 9: 6: 4: 3: 2: 521: 510: 507: 506: 504: 495: 492: 490: 487: 486: 482: 473: 469: 465: 461: 457: 450: 447: 442: 438: 433: 428: 424: 420: 416: 408: 405: 400: 396: 392: 388: 384: 380: 372: 369: 358: 354: 348: 345: 340: 336: 332: 326: 323: 319: 317:9780122267659 313: 309: 305: 301: 297: 296: 290: 282: 279: 274: 270: 266: 262: 257: 252: 248: 244: 240: 233: 231: 229: 227: 225: 221: 216: 212: 207: 202: 198: 194: 190: 183: 180: 173: 171: 164: 162: 159: 157: 149: 147: 145: 141: 137: 133: 129: 125: 124:neuraminidase 121: 120:hemagglutinin 117: 116:glycoproteins 113: 104: 97: 95: 93: 89: 88:cell mediated 80: 78: 76: 75:neuraminidase 72: 68: 64: 63:glycoproteins 59: 51: 49: 47: 42: 38: 34: 30: 21: 463: 459: 449: 422: 418: 407: 382: 378: 371: 360:. Retrieved 356: 347: 335:Merck source 334: 325: 294: 281: 246: 242: 196: 192: 182: 168: 160: 153: 136:nucleocapsid 128:phospholipid 109: 84: 55: 28: 26: 509:Vaccination 385:: S26–38. 362:2019-01-03 289:"Antigens" 174:References 265:1846-9558 215:2250-1177 122:(HA) and 112:liposomes 503:Category 472:11809693 441:21315623 419:Immunity 399:16026906 339:Archived 273:26011928 29:virosome 379:Vaccine 300:201–207 67:antigen 41:Viruses 37:vesicle 470:  439:  397:  314:  271:  263:  213:  73:, and 46:vector 156:HIV-1 144:virus 31:is a 468:PMID 437:PMID 395:PMID 312:ISBN 269:PMID 261:ISSN 211:ISSN 90:and 427:doi 387:doi 304:doi 251:doi 201:doi 505:: 464:62 462:. 458:. 435:. 423:34 421:. 417:. 393:. 383:23 381:. 355:. 337:. 333:. 310:, 302:, 292:, 267:. 259:. 247:65 245:. 241:. 223:^ 209:. 195:. 191:. 146:. 69:, 27:A 474:. 443:. 429:: 401:. 389:: 375:h 365:. 306:: 275:. 253:: 217:. 203:: 197:3

Index


drug or vaccine delivery mechanism
vesicle
Viruses
vector
phospholipid mono/bilayer
glycoproteins
antigen
haemagglutinin
neuraminidase
cell mediated
humoral immune responses

liposomes
glycoproteins
hemagglutinin
neuraminidase
phospholipid
influenza virus
nucleocapsid
genetic material
virus
HIV-1
"A Multipurpose and Novel Carrier for Drug Delivery and Targeting - Virosomes"
doi
10.22270/jddt.v3i5.627
ISSN
2250-1177

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