The Brigham and Women's Hospital, Inc.

The Charles Stark Draper Laboratory, Inc.

Mind Medicine, Inc.

Massachusetts Institute of Technology

Peter Mack

Jeffrey T Borenstein

Eli J Weinberg

Guillermo Garcia-Cardena

Ahmad S Khalil

Malinda M Tupper

Sarah L Tao

Jon Schroeder

Jason Oliver Fiering

Ernest Soonho Kim

William J Adams, Jr

Bethany Amber Doty

Dustin Melton

Timm Trenktrog

Lisa Marie Garrett

Gerald S Jones

Stephen L Bellio

Mitchell L Hansberry

Stephen E Schneider

James Ching-Ming Hsiao

Sarah Tao

Robert Barrow

William James Adams

A solid oral immediate release formulation of LSD, wherein the composition is produced by lyophilization of a feedstock in a pre-formed mold to form an orally disintegrating tablet. A method of making a solid oral immediate release formulation of LSD by lyophilizing a flash frozen stock solution of LSD and excipients, including a non-gelling matrix former, filler, and binder in a pre-formed mold, and forming an orally disintegrating tablet. A method of treating an individual by administering a solid oral immediate release formulation of LSD, wherein the composition is produced by lyophilization of a feedstock in a pre-formed mold to form an orally disintegrating tablet and treating the individual.

Lyophilized orally disintegrating tablet formulations of d-lysergic acid diethylamide for therapeutic applications

A composition of psilocin that is stable including at least one agent or chemical modification that provides enhanced stability. A method making stable psilocin, by providing a formulation of psilocin including at least one agent or chemical modification that provides enhanced stability. A method of treatment of a disease or condition, by administering a composition of psilocin that is stable to an individual and treating the disease or condition.

Formulations of psilocin that have enhanced stability

Microfluidic structures featuring substantially circular channels may be fabricated by embossing polymer sheets.

Microfluidic structures for biomedical applications

The systems and methods described herein relate to a high-throughput flow apparatus. The apparatus is used with an array of wells, and is configured to impart a predetermined shear stress on cells cultured within each of the wells of the array of wells. The apparatus includes a plurality of mechanical tips. The plurality of mechanical tips each includes a head with a hemispheroid shape. The apparatus also includes a motor associated with at least one of plurality of mechanical tips. The motor is configured to drive the plurality of mechanical tips to impart the shear stress pattern in each of the wells.

Systems and method for high-throughput testing

microfluidic structures for biomedical applications

A high-throughput flow system includes an array of wells and a separate mechanical tip positioned within each well. Each mechanical tip is separately actuated to impart a shear stress pattern. A separate sleeve may be associated with each tip for maintaining a predetermined distance between the tip and a floor of the tip's corresponding well, with each tip being rotatable within its corresponding sleeve. Alternatively, a separate post may be associated with each tip for maintaining a predetermined distance between the tip and a floor of the tip's corresponding well, with each tip being rotatable about its corresponding post.

High-throughput biological screening

Methods of fabricating microfluidic structures featuring substantially circular channels are provided. The methods involve (a) providing a patterned wafer comprising at least one exposed electrically conductive region and at least one exposed electrically insulating region; (b) electroplating an inverse channel portion with substantially semicircular cross section onto the wafer, thereby forming a first master mold; (c) employing the first master mold so as to emboss a channel portion in a first polymer sheet; and (d) aligning and bonding the first polymer sheet with a second polymer sheet having a corresponding channel portion such as to define a first channel with substantially circular cross section between the polymer sheets.

Method of fabricating microfluidic structures for biomedical applications

Growing community of inventors

Chapel Hill, NC, United States of America

Peter Mack