Tesis
Annona Mucosa (Annonaceae) para o controle de pragas: estudo fitoquímico biomonitorado, síntese de mímicos e desenvolvimento de processos de nanoencapsulação
Fecha
2016-02-26Registro en:
Autor
Bicalho, Keylla Utherdyany
Institución
Resumen
Annona mucosa (ANNONACEAE) https://repositorio.ufscar.br/FOR PESTS CONTROL: BIOASSAY-GUIDED
PHYTOCHEMICAL STUDY, SYNTHESIS OF MIMICS AND DEVELOPMENT OF
NANOENCAPSULATION PROCESSES – The agriculture is one of the major drivers
of Brazilian GDP. However, several losses have occurred during the agricultural
productive process, especially the pest attack. Currently, leaf-cutting ants and the
maize weevil have caused great economics losses and are hard to control. One
alternative for these pests control is searching on nature for novel compounds with
insecticide and fungicide potential. In this perspective, the first part of this work was
the biassay-guided phytochemical study of Annona mucosa, searching for novel
compounds with these properties. From the vegetal parts crude extracts, was verified
great insecticide and fungicide potentials for its fractions. The phytochemical study of
leaves and seeds crude extracts resulted on the isolation and identification of 11
secondary metabolites, 3 lignans, 4 acetogenins and 4 flavonoids, and confirmed the
biological potential of these substances. Acetogenins are derived from fatty acid and
are characterized by the presence of two main cores, diol-THF group and a α,β-
unsaturated-γ-lactone separated by an alkyl chain. Several researches aiming the
acetogenins mimics total synthesis, with simplified structures, but keeping the
biologically important functionalities, have been developed. Based on this idea, the
second part of this work aimed the total synthesis of rolliniastatin-1 mimics, major
acetogenin on the A. mucosa chemical composition. A complete synthetic route with
12 steps was developed in order to get the polyether mimics. Although, only one
complete mimic was synthesized, the synthetic rout was completely established and a
new simple methodology of sequential vinyl ether exchange-Claisen Rearrangement
was employed for the synthesis of γ,δ–unsaturated aldehydes. Besides, the key step,
the oxidative cyclization, reaction for treo-cis-treo THF ring formation, was optimized
by its yields and stereoselectivity. In the quest for developing new technologies for
bioactive compounds application, the nanoencapsulaiton is a technique that results in
controlled release systems of these substances and can be applied in several fields.
In this way, the last part of this work was about the formulation development and
improvement of process and parameters for the nanoencapsulation of the furofuranic
lignan sesamin. To achieve that, a 23 factorial design was performed, where were
evaluated the effect of the independent variables (type and amount of polymer and amount of oil) on the nanoparticles physical-chemistry characteristics and on the
trapping, recovery and release rates. The biopolymers poly- ε-caprolactone and lignin
were employed and colloidal suspensions of nanocapsules and nanospheres were
prepared. The results from the factorial design proved the efficiency of both
biopolymers and the best nanoformulation was the nanospheres suspension produced
with 100 mg of lignina (NF3). The wide availability of lignin, which is an industrial
residue, its non-toxicity to the environment and the technological application reported
make this biopolymer a great potential for use in agricultural field.