3 research outputs found
Polymer Encapsulation of an Amorphous Pharmaceutical by initiated Chemical Vapor Deposition for Enhanced Stability
The
usage of amorphous solids in practical applications, such as in medication,
is commonly limited by the poor long-term stability of this state,
because unwanted crystalline transitions occur. In this study, three
different polymeric coatings are investigated for their ability to
stabilize amorphous films of the model drug clotrimazole and to protect
against thermally induced transitions. For this, drop cast films of
clotrimazole are encapsulated by initiated chemical vapor deposition
(iCVD), using perfluorodecyl acrylate (PFDA), hydroxyethyl methacrylate
(HEMA), and methacrylic acid (MAA). The iCVD technique operates under
solvent-free conditions at low temperatures, thus leaving the solid
state of the encapsulated layer unaffected. Optical microscopy and
X-ray diffraction data reveal that at ambient conditions of about
22 °C, any of these iCVD layers extends the lifetime of the amorphous
state significantly. At higher temperatures (50 or 70 °C), the
p-PFDA coating is unable to provide protection, while the p-HEMA and
p-MAA strongly reduce the crystallization rate. Furthermore, p-HEMA
and p-MAA selectively facilitate a preferential alignment of clotrimazole
and, interestingly, even suppress crystallization upon a temporary,
rapid temperature increase (3 °C/min, up to 150 °C). The
results of this study demonstrate how a polymeric coating, synthesized
directly on top of an amorphous phase, can act as a stabilizing agent
against crystalline transitions, which makes this approach interesting
for a variety of applications
Solvent Vapor Annealing of Amorphous Carbamazepine Films for Fast Polymorph Screening and Dissolution Alteration
Solubility
enhancement and thus higher bioavailability are of great
importance and a constant challenge in pharmaceutical research whereby
polymorph screening and selection is one of the most important tasks.
A very promising approach for polymorph screening is solvent vapor
annealing where a sample is exposed to an atmosphere saturated with
molecules of a specific chemical/solvent. In this work, amorphous
carbamazepine thin films were prepared by spin coating, and the transformation
into crystalline forms under exposure to solvent vapors was investigated.
Employing grazing incidence X-ray diffraction, four distinct carbamazepine
polymorphs, a solvate, and hydrates could be identified, while optical
microscopy showed mainly spherulitic morphologies. <i>In vitro</i> dissolution experiments revealed different carbamazepine release
from the various thin-film samples containing distinct polymorphic
compositions: heat treatment of amorphous samples at 80 °C results
in an immediate release; samples exposed to EtOH vapors show a drug
release about 5 times slower than this immediate one; and all the
others had intermediate release profiles. Noteworthy, even the sample
of slowest release has a manifold faster release compared to a standard
powder sample demonstrating the capabilities of thin-film preparation
for faster drug release in general. Despite the small number of samples
in this screening experiment, the results clearly show how solvent
vapor annealing can assist in identifying potential polymorphs and
allows for estimating their impact on properties like bioavailability
Growth Regimes of Poly(perfluorodecyl acrylate) Thin Films by Initiated Chemical Vapor Deposition
Control over thin film growth (e.g.,
crystallographic orientation
and morphology) is of high technological interest as it affects several
physicochemical material properties, such as chemical affinity, mechanical
stability, and surface morphology. The effect of process parameters
on the molecular organization of perfluorinated polymers deposited
via initiated chemical vapor deposition (iCVD) has been previously
reported. We showed that the tendency of polyÂ(1<i>H</i>,1<i>H</i>,2<i>H</i>,2<i>H</i>-perfluorodecyl
acrylate) (pPFDA) to organize in an ordered lamellar structure is
a function of the filament and substrate temperatures adopted during
the iCVD process. In this contribution, a more thorough investigation
of the effect of such parameters is presented, using synchrotron radiation
grazing incidence and specular X-ray diffraction (GIXD and XRD) and
atomic force microscopy (AFM). The parameters influencing the amorphization,
mosaicity, and preferential orientation are addressed. Different growth
regimes were witnessed, characterized by a different surface structuring
and by the presence of particular crystallographic textures. The combination
of morphological and crystallographic analyses allowed the identification
of pPFDA growth possibilities between island or columnar growth