ES2517040B2 - Nanoparticles for the controlled release of active ingredients - Google Patents

Nanoparticles for the controlled release of active ingredients Download PDF

Info

Publication number
ES2517040B2
ES2517040B2 ES201330625A ES201330625A ES2517040B2 ES 2517040 B2 ES2517040 B2 ES 2517040B2 ES 201330625 A ES201330625 A ES 201330625A ES 201330625 A ES201330625 A ES 201330625A ES 2517040 B2 ES2517040 B2 ES 2517040B2
Authority
ES
Spain
Prior art keywords
nanoparticles
active ingredient
active ingredients
controlled release
hyaluronic acid
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Fee Related
Application number
ES201330625A
Other languages
Spanish (es)
Other versions
ES2517040A1 (en
Inventor
Laura CALDERÓN MUÑOZ
Ruth EXPÓSITO HARRIS
Niuris Acosta Contreras
Ángeles María Heras Caballero
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
INNOVACIONES FISICAS Y QUIMICAS SOSTENIBLES SL
INNOVACIONES FISICAS Y QUIMICAS SOSTENIBLES S L
Innovaciones Fisicas Y Quimicas Sostenibles Sl
Original Assignee
INNOVACIONES FISICAS Y QUIMICAS SOSTENIBLES SL
INNOVACIONES FISICAS Y QUIMICAS SOSTENIBLES S L
Innovaciones Fisicas Y Quimicas Sostenibles Sl
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by INNOVACIONES FISICAS Y QUIMICAS SOSTENIBLES SL, INNOVACIONES FISICAS Y QUIMICAS SOSTENIBLES S L, Innovaciones Fisicas Y Quimicas Sostenibles Sl filed Critical INNOVACIONES FISICAS Y QUIMICAS SOSTENIBLES SL
Priority to ES201330625A priority Critical patent/ES2517040B2/en
Publication of ES2517040A1 publication Critical patent/ES2517040A1/en
Application granted granted Critical
Publication of ES2517040B2 publication Critical patent/ES2517040B2/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/48Preparations in capsules, e.g. of gelatin, of chocolate
    • A61K9/50Microcapsules having a gas, liquid or semi-solid filling; Solid microparticles or pellets surrounded by a distinct coating layer, e.g. coated microspheres, coated drug crystals
    • A61K9/51Nanocapsules; Nanoparticles
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B82NANOTECHNOLOGY
    • B82YSPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y5/00Nanobiotechnology or nanomedicine, e.g. protein engineering or drug delivery

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Health & Medical Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Nanotechnology (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Health & Medical Sciences (AREA)
  • Biophysics (AREA)
  • Biomedical Technology (AREA)
  • Molecular Biology (AREA)
  • General Engineering & Computer Science (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Biotechnology (AREA)
  • Physics & Mathematics (AREA)
  • Medical Informatics (AREA)
  • Optics & Photonics (AREA)
  • Epidemiology (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Cosmetics (AREA)

Abstract

Nanopartículas para la liberación controlada de ingredientes activos, las cuales comprenden quitosano, ácido hialurónico y colágeno y además incorporan un ingrediente activo; un procedimiento para la obtención de dichas nanopartículas, el cual implica la transformación de una fase líquida, que contiene los polímeros en una fase sólida, que a su vez contiene el ingrediente activo que cumple con la forma requerida para ser administrada con un perfil de liberación controlada y que, además, permite la incorporación directa del ingrediente activo preservando su integridad o acción terapéutica, y uso de las nanopartículas para la fabricación de composiciones farmacéuticas o cosméticas.Nanoparticles for the controlled release of active ingredients, which comprise chitosan, hyaluronic acid and collagen and also incorporate an active ingredient; a process for obtaining said nanoparticles, which involves the transformation of a liquid phase, which contains the polymers in a solid phase, which in turn contains the active ingredient that complies with the form required to be administered with a release profile controlled and that, in addition, allows the direct incorporation of the active ingredient preserving its integrity or therapeutic action, and use of nanoparticles for the manufacture of pharmaceutical or cosmetic compositions.

Description



imagen1image 1

imagen2image2

imagen3image3

imagen4image4

imagen5image5

imagen6image6

imagen7image7

imagen8image8

imagen9image9

imagen10image10

imagen11image11

imagen12image12

imagen13image13

imagen14image14

P201330625 P201330625

30-04-2013 04-30-2013

Figura 5: Gráfico de % de liberación de antioxidantes vs. tiempo (horas), a partir de nanopartículas que comprenden quitosano, ácido hialurónico y colágeno con un 20% de extracto de hojas de olivo encapsulado, según unas formulaciones a), b), c) y d), que corresponden respectivamente a relaciones en masa de 9:1:2, 2:1:9, 1:1:2 y 2:3:6. Figure 5: Chart of% antioxidant release vs. time (hours), from nanoparticles comprising chitosan, hyaluronic acid and collagen with 20% encapsulated olive leaf extract, according to formulations a), b), c) and d), which correspond respectively to mass ratios of 9: 1: 2, 2: 1: 9, 1: 1: 2 and 2: 3: 6.

EJEMPLOS En los ejemplos de la presente invención se emplean las siguientes abreviaturas: HCS: Hidrocloruro de quitosano HA: Ácido hialurónico Col: Colágeno TPP: Tripolifosfato sódico BSA: Albúmina de suero bovino OLE: Extracto de hojas de olivo NPs: Nanopartículas EXAMPLES In the examples of the present invention the following abbreviations are used: HCS: Chitosan hydrochloride HA: Hyaluronic acid Col: Collagen TPP: Sodium tripolyphosphate BSA: Bovine serum albumin OLE: Olive leaf extract NPs: Nanoparticles

Ejemplo 1 Se prepararon nanopartículas de hidrocloruro de quitosano, ácido hialurónico y colágeno, utilizando tripolifosfato sódico como agente entrecruzante. Se adicionó la disolución de ácido hialurónico (3 mg/ml) y tripolifosfato sódico (0,1%) sobre la disolución que contiene hidrocloruro de quitosano (0,15%), bajo agitación constante y durante 10 minutos, permitiendo la estabilización de las nanopartículas generadas. Se procedió a la centrifugación de éstas con objeto de eliminar los posibles residuos de quitosano y ácido hialurónico sin reaccionar y el pellet resultante se vuelve a suspender en una disolución de colágeno (5 mg/ml) durante 2 horas, en agitación constante. Posteriormente, se añadió una cantidad adecuada de tripolifosfato sódico y se deja reaccionar 30 minutos, permitiendo la completa evolución del sistema hasta la obtención de nanopartículas estables. Una vez preparadas, se midió su diámetro medio (nm), así como su carga eléctrica superficial y se estudió su morfología mediante microscopía electrónica de transmisión. En la tabla 1, para todo el rango de concentraciones y en las figuras 1 y 4, para unas concentraciones deterrminadas, se muestran algunos de los valores que toman los parámetros citados en función de la proporción de HCS, HA, Col y TPP utilizados. Example 1 Chitosan hydrochloride, hyaluronic acid and collagen nanoparticles were prepared, using sodium tripolyphosphate as the crosslinking agent. The solution of hyaluronic acid (3 mg / ml) and sodium tripolyphosphate (0.1%) was added to the solution containing chitosan hydrochloride (0.15%), under constant stirring and for 10 minutes, allowing the stabilization of the generated nanoparticles. The centrifugation of these was carried out in order to eliminate the possible unreacted chitosan and hyaluronic acid residues and the resulting pellet is resuspended in a collagen solution (5 mg / ml) for 2 hours, under constant stirring. Subsequently, an adequate amount of sodium tripolyphosphate was added and allowed to react for 30 minutes, allowing the complete evolution of the system until obtaining stable nanoparticles. Once prepared, its average diameter (nm) was measured, as well as its surface electric charge and its morphology was studied by transmission electron microscopy. Table 1, for the entire range of concentrations and in Figures 1 and 4, for certain concentrations determined, some of the values that take the parameters mentioned according to the proportion of HCS, HA, Col and TPP used are shown.

Tabla 1 Table 1

9 9

imagen15image15

imagen16image16

imagen17image17

imagen18image18

imagen19image19

imagen20image20

imagen21image21

imagen22image22

imagen23image23

Claims (1)



imagen1image 1 imagen2image2 imagen3image3 imagen4image4 imagen5image5
ES201330625A 2013-04-30 2013-04-30 Nanoparticles for the controlled release of active ingredients Expired - Fee Related ES2517040B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
ES201330625A ES2517040B2 (en) 2013-04-30 2013-04-30 Nanoparticles for the controlled release of active ingredients

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
ES201330625A ES2517040B2 (en) 2013-04-30 2013-04-30 Nanoparticles for the controlled release of active ingredients

Publications (2)

Publication Number Publication Date
ES2517040A1 ES2517040A1 (en) 2014-10-31
ES2517040B2 true ES2517040B2 (en) 2015-04-29

Family

ID=51795080

Family Applications (1)

Application Number Title Priority Date Filing Date
ES201330625A Expired - Fee Related ES2517040B2 (en) 2013-04-30 2013-04-30 Nanoparticles for the controlled release of active ingredients

Country Status (1)

Country Link
ES (1) ES2517040B2 (en)

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU4476600A (en) * 1999-04-22 2000-11-10 Vanderbilt University Polymeric encapsulation system promoting angiogenesis

Also Published As

Publication number Publication date
ES2517040A1 (en) 2014-10-31

Similar Documents

Publication Publication Date Title
WO2019036008A8 (en) Lipids for use in lipid nanoparticle formulations
Fathalla et al. In-vitro and in-vivo evaluation of niosomal gel containing aceclofenac for sustained drug delivery
EA201591003A1 (en) DERIVATIVES OF BORONIC ACID AND THEIR THERAPEUTIC APPLICATION
MX2013013401A (en) Controlled release peptide formulations.
CO6612270A2 (en) Method for preparing an enteric hard capsule and enteric hard capsule prepared by it
AR105203A1 (en) SOLID ORAL FORMULATION CONTAINING IRINOTECAN AND METHOD OF PREPARATION OF THE SAME
PH12016501519A1 (en) Solid pharmaceutical compositions comprising biopterin derivatives and uses of such compositions
MX346661B (en) Stabilized eperisone medical composition, and sustained-release preparation containing same.
PE20171246A1 (en) PHARMACEUTICAL FORMULATIONS THAT INCLUDE HIGH PURITY CANGRELOR AND METHODS FOR THE PREPARATION AND USE OF SAME
EA202092926A2 (en) LYOPHILIZED COMPOSITIONS CONTAINING FACTOR IX
EA201991023A1 (en) PHARMACEUTICAL COMPOSITION FOR Parenteral Administration Containing Karglum Acid
WO2016040814A3 (en) Disulfide polymers and methods of use
ES2517040B2 (en) Nanoparticles for the controlled release of active ingredients
JP2015511618A5 (en)
PH12015502717A1 (en) Anti-fibrogenic compounds, methods and uses thereof
MX2020005921A (en) Formulations and methods for vaginal delivery of antiprogestins.
RU2017141462A (en) COMPOSITION CONTAINING NORBIXIN FOR PROTECTION OF CELL PIGMENT EPITHELIUM CELLS
JP2016507535A5 (en)
RU2015145451A (en) PRODUCTS FOR LOCAL USE CONTAINING HYALURONIC ACID, VERBASCOZIDE AND GLYCEROPHOSPHOINOSITOL
MX2020002347A (en) Use of physiological cooling active ingredients, and compositions comprising such active ingredients.
CN103751214A (en) Alligator oil nano-liposome and preparation method thereof
ZA201905738B (en) Conjugate of salicylic acid and peptide
MX370974B (en) Preparation of zinc citrate and of zinc citrate-containing oral care compositions.
CA2903759C (en) Concentrated aqueous azalide formulations
TAN Preparation, characteristic and in vivo study of H102 loaded PEG-PLGA nanoparticles

Legal Events

Date Code Title Description
FG2A Definitive protection

Ref document number: 2517040

Country of ref document: ES

Kind code of ref document: B2

Effective date: 20150429

FD2A Announcement of lapse in spain

Effective date: 20220701