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公开(公告)号:US09855217B2
公开(公告)日:2018-01-02
申请号:US15023110
申请日:2014-09-18
Inventor: C. Jeffrey Brinker , Yu-Shen Lin
IPC: A61K9/14 , A61K9/127 , A61K31/7088 , B82Y5/00 , A61K9/51 , A61K38/16 , A61K38/43 , A61K39/395 , C12N15/88 , B82Y15/00
CPC classification number: A61K9/1271 , A61K9/14 , A61K9/5115 , A61K9/5123 , A61K31/7088 , A61K38/16 , A61K38/43 , A61K39/395 , B82Y5/00 , B82Y15/00 , C12N15/88
Abstract: In one aspect, the invention provides novel monodisperse, colloidally-stable, toroidal mesoporous silica nanoparticles (TMSNPs) which are synthesized from ellipsoid-shaped mesoporous silica nanoparticles (MSNPs) which are prepared using an ammonia basecatalyzed method under a low surfactant conditions. Significantly, the TMSNPs can be loaded simultaneously with a small molecule active agent, a siRNA, a mRNA, a plasmid and other cargo and can be used in the diagnosis and/or treatment of a variety of disorders, including a cancer, a bacterial infection and/or a viral infection, among others. Related protocells, pharmaceutical compositions and therapeutic and diagnostic methods are also provided.
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公开(公告)号:US11045554B1
公开(公告)日:2021-06-29
申请号:US16443316
申请日:2019-06-17
Inventor: Oscar Negrete , C. Jeffrey Brinker , Torri Rinker , Annette Estelle LaBauve
IPC: A61K31/4965 , A61K47/69 , A61K47/54 , A61K31/517
Abstract: The present invention relates to lipid-coated particles for treating viral infections, including viral encephalitis infections. In particular, an antiviral compound can be disposed within the lipid-coated particle, thereby providing an antiviral carrier. Methods of making and using such carriers are described herein.
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公开(公告)号:US09605344B2
公开(公告)日:2017-03-28
申请号:US14917566
申请日:2014-09-12
Applicant: STC.UNM
Inventor: Ying-Bing Jiang , Joseph L. Cecchi , Yaqin Fu , C. Jeffrey Brinker
IPC: C23C16/455 , C23C16/46
CPC classification number: C23C16/45525 , C23C16/45534 , C23C16/46
Abstract: An atomic layer deposition method is disclosed for preparing polypeptides. The method comprises providing a solid-phase support comprising a reactive amine monolayer in an atomic layer deposition (ALD) chamber. The solid-phase support is contacted with a first protected amino acid substituted with a protecting group by atomic layer deposition, wherein the protecting group is bonded to a non-side chain amino group of the protected amino acid. A carboxylic acid group of the first protected amino acid is reacted with the reactive amine monolayer, thereby coupling the first protected amino acid to the solid-phase support to produce a coupled-product.
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