Details for Patent: 6,652,885

Title:	Purification and stabilization of peptide and protein pharmaceutical agents
Abstract:	Methods are provided for purifying peptides and proteins by incorporating the peptide or protein into a diketopiperazine or competitive complexing agent to facilitate removal one or more impurities, i.e. undesirable components, from the peptide or protein. In a preferred embodiment, a peptide, such as insulin, containing one or more impurities, e.g., zinc ions, is entrapped in diketopiperazine to form a precipitate of peptide/diketopiperazine/impurity, which is then washed with a solvent for the impurity to be removed, which is a nonsolvent for the diketopiperazine and a nonsolvent for the peptide. Formulations and methods also are provided for the improved transport of active agents across biological membranes, resulting for example in a rapid increase in blood agent concentration. The formulations include microparticles formed of (i) the active agent, which may be charged or neutral, and (ii) a transport enhancer that masks the charge of the agent and/or that forms hydrogen bonds with the target biological membrane in order to facilitate transport. In a preferred embodiment, insulin is administered via the pulmonary delivery of microparticles comprising fumaryl diketopiperazine and insulin in its biologically active form. The charge on the insulin molecule is masked by hydrogen bonding it to the diketopiperazine, thereby enabling the insulin to pass through the target membrane. This method of delivering insulin results in a rapid increase in blood insulin concentration that is comparable to the increase resulting from intravenous delivery.
Inventor(s):	Steiner; Solomon S. (Mount Kisco, NY), Woods; Rodney J. (New Hampton, NY), Sulner; Joseph W. (Paramus, NJ)
Assignee:	MannKind Corporation (Danbury, CT)
Filing Date:	Aug 20, 2002
Application Number:	10/224,761
Claims:	1. A method for delivering insulin to a patient in need thereof, comprising administering to the patient an effective amount of the insulin in a composition which comprises microparticles of a diketopiperazine in which monomeric or dimeric insulin is complexed to the diketopiperazine. 2. The method of claim 1 wherein the diketopiperazine is fumaryl diketopiperazine. 3. The method of claim 2 wherein the composition is in a dry powder form administered to the lungs via inhalation. 4. The method of claim 1 wherein the patient is a Type II diabetic. 5. The method of claim 4 wherein the composition is administered concurrently with, or less than about 20 minutes prior to, the patient eating a meal. 6. The method of claim 1 wherein the composition is provided in one or more unit doses of insulin, each dose equivalent to about 6 IU of insulin.