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In‐Solution Structural Considerations by 1 H NMR and Solid‐State Thermal Properties of Inulin‐ d ‐α‐Tocopherol Succinate (INVITE) Micelles as Drug Delivery Systems for Hydrophobic Drugs
Author(s) -
Catenacci Laura,
Mandracchia Delia,
Sorrenti Milena,
Colombo Lino,
Serra Massimo,
Tripodo Giuseppe
Publication year - 2014
Publication title -
macromolecular chemistry and physics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.57
H-Index - 112
eISSN - 1521-3935
pISSN - 1022-1352
DOI - 10.1002/macp.201400342
Subject(s) - micelle , amphiphile , thermogravimetric analysis , polymer , chemistry , thermal stability , drug delivery , chemical engineering , crystallinity , polymer chemistry , organic chemistry , drug carrier , copolymer , aqueous solution , crystallography , engineering
1 H NMR is a suitable method to clarify the kind of interactions leading to the self‐assembly of amphiphilic polymers. This work shows, from 1 H NMR studies performed in solution, that the self‐assembly ability of the synthesized Inulin‐ d ‐α‐tocopherol succinate (INVITE) amphiphilic polymers, can be addressed to specific π–π interactions between the aromatic regions of d ‐α‐tocopherol. This result suggests the use of INVITE systems for the preferential loading of aromatic group bearing drugs such as curcumin. The preparation conditions, effect of drug loading, and lyophilization on the INVITE systems are evaluated by DSC and thermogravimetric analysis (TGA) analysis to assess whether common pharmaceutical processes could influence the physical properties of the amphiphilic polymers, such as crystallinity, glass‐transition temperature or thermal degradation, to predict the physical stability of the systems upon administration. Furthermore, the size stability of the micelle systems up to 60 days is monitored to assess the feasibility of the INVITE micelles’ long‐term storage upon reconstitution with water.