摘要:
Delivery system for active ingredients which comprises lipid nanoparticles, such as solid lipid nanoparticles (SLN) or nanostructured lipid carriers (NLC), polymerically coated, and their use in the preparation of pharmaceutical, cosmetic and/or alimentary compositions.
摘要:
The present invention relates to a process for obtaining compositions constituted by propolis nanoparticles and to the use thereof, said nanoparticles being optionally associated to one or more substances of interest such as active ingredients, as well as, optionally, substances of secondary effect such as synergists and adjuvants. The process for obtaining the nanoparticles comprises the steps of preparing a fraction A, which consists of propolis extract dissolved in an organic solvent, to which one or m ore stabilizers and/or emulsifiers may be added, as well as, optionally, one or more substances of interest and/or of secondary effect; ii) preparing a fraction B, aqueous phase, constituted by: (ii.1) water; or (ii.2) an aqueous solution or dispersion, to which one or more stabilizers and/or emulsifiers may be added; (iii) drooping the fraction A onto the fraction B or the fraction B onto the fraction A; iv) homogenizing the mixture by mechanical stirring and spontaneous formation of nanoaprticles with average size ranging from 1 to 1000 nm in a dispersion; v) optionally the following additional steps may be involved: (v-1) removing the organic solvent/ and/or (v-2) drying the nanodispersion. The developed compositions have applications in fields such as agrochemical, pharmaceutical, cosmetic or chemical fields.
摘要:
The present invention pertains to therapeutic compositions and delivery systems comprising at least one microparticle or nanoparticle. In various embodiments, the surface of the microparticle or nanoparticle is modified or functionalized with at least a portion of an isolated cellular membrane, such as an isolated plasma membrane. In addition, the microparticle or nanoparticle contains at least one active agent, such as a therapeutic and/or imaging agent. In additional embodiments, the compositions and delivery systems of the present invention may be used for targeted delivery of an active agent. Also provided are methods of making the therapeutic compositions and delivery systems of the present invention.
摘要:
Delivery system for active ingredients which comprises lipid nanoparticles, such as solid lipid nanoparticles (SLN) or nanostructured lipid carriers (NLC), polymerically coated, and their use in the preparation of pharmaceutical, cosmetic and/or alimentary compositions.
摘要:
Described are a method and a composition for delivery of a protein to an antigen presenting cell. The composition is composed of a polypeptide component, a buffering component and a particle to be phagocytized. In one embodiment, the antigen presenting cell is aa macrophage or a dendritic cell and the particle to be phagocytized is from a natural source, such as from a microbial source. The composition itself, or cells pretreated with the composition, are useful for strategies in vaccine development.
摘要:
Compositions comprising liposomes composed of whole cell membrane fraction are provided. The liposomes may be attached to, or encapsulate a pharmaceutical agent. Also provided are methods of generating and using these liposomes.
摘要:
The present invention provides solution to the problem involved in delivery of active molecules to nucleus. More particularly, the invention provides intrinsically fluorescent and inherently surface functionalized carbon nanospheres which are non-toxic. Also, these carbon nanospheres [CSP] were adsorbed with CTPB [CSP-CTPB] and the adsorbed CSP-CTPB are permeable to cells with nuclear targeting ability. In addition, the present invention provides a composition, a process to prepare the composition comprising CSP with adsorbed active/ therapeutic molecules. Further, the instant invention provides a method for delivering active molecules inside a cell nucleus.
摘要:
An encapsulated microparticle composition and its method of use in drug delivery and diagnostic applications are disclosed. Also disclosed are methods of storing and administering drug compounds at high concentration in condensed-phase microparticles.