Abstract:
Polymeric conjugates comprising a polymeric matrix having associated therewith an agent that down-regulates an activity or expression of a polypeptide associated with onset or progression of melanoma, and optionally and preferably, an additional agent that acts in synergy with said agent, are provided. Synthetic methodologies for preparing these conjugates and uses thereof in treating melanoma and other cancerous diseases are also provided.
Abstract:
Polymeric conjugates comprising a polymeric matrix having associated therewith an agent that down-regulates an activity or expression of a polypeptide associated with onset or progression of melanoma, and optionally and preferably, an additional agent that acts in synergy with said agent, are provided. Synthetic methodologies for preparing these conjugates and uses thereof in treating melanoma and other cancerous diseases are also provided.
Abstract:
Wireless and non-wireless drug delivery integrated circuits, systems, and methods of delivering therapeutic pharmaceutical compounds are provided. The system can include a control module, a wireless drug delivery integrated circuit, a first electrode and a second electrode that are both attached to the wireless drug delivery integrated circuit, an electroactive polymer, and a pharmaceutical compound. The electroactive polymer and the pharmaceutical compound can be formed as films on one of the electrodes and, when placed in a solution, a voltage potential can be applied across the electrodes causing the pharmaceutical compound to be released into the solution.
Abstract:
본 발명은 항암제 및 인도시아닌 그린이 캡슐화된 리포좀 복합체를 포함하는 암 치료용 조성물 및 이의 제조방법에 관한 것으로, 구체적으로는 리포좀, 항암제 및 인도시아닌그린을 포함하는 복합체를 포함하고, 치료적으로 유효한 광 조사시 발생하는 인도시아닌 그린에 의한 광열효과와 항암제에 의한 암 치료효능을 동시에 가지는 암 치료용 조성물 및 이를 제조할 수 있는 방법에 관한 것이다.
Abstract:
본 발명은 수상에서 음이온성 약물과 양이온성 화합물을 정전기적 결합을 이용하여 나노입자를 형성시키는 단계; 및 상기 나노입자를 양친성 고분자 및 임의로 폴리락트산염으로 이루어진 고분자 미셀 안에 포함시키는 단계를 포함함으로써, 정전기적 결합과 소수성 결합을 증가시켜 제형의 음이온 약물 봉입률을 높임으로써 음이온성 약물 전달용 조성물의 제조 수득률을 증가시키는 제조 방법에 관한 것이다.
Abstract:
The present application relates to a pharmaceutical composition for transmucosal administration of an active lipophilic compound through the oral mucosa comprising a lipophilic active compound, a polymeric matrix formed by two or more water-soluble polymers and a rapid dissolution agent. At least one of the water-soluble polymers is an amphiphilic polymer and at least one is either a hydrophilic polymer or an amphiphilic polymer with a hydrophobic-hydrophilic balance different from the first amphiphilic polymer. In addition, the polymeric matrix is not crosslinked and no covalent interaction occurs between the two or more polymers and between the polymers and the lipophilic active compound, which is interwoven with the aforesaid polymeric matrix.
Abstract:
Disclosed are injectable, biodegradable neuroscaffolds formed in situ by self-assembling biodegradable polymeric microparticles, nanoparticles, or any combination thereof, via copper-free click chemistry or Michael-type addition coupling reactions. The injectable, biodegradable neuroscaffolds provide 3-D structural support, neuroprotection, and/or subsequent regeneration in a subject with a spinal cord injury or a focal neurological disorder.
Abstract:
The present disclosure relates to a pharmaceutical composition comprising dutasteride and propylene glycol monolaurate, and a capsule formulation comprising the same.
Abstract:
Methods of labeling, identifying and differentiating microorganisms using functionalized Buckyballs are provided herein. The invention further provides methods for imaging or inhibiting gene expression using functionalized Buckyballs of the invention. The invention also provides a system for labeling, identifying and differentiating microorganisms.