banner
home azienda prodotti anatomia contatti
integratori
ombra_sx
line
down
icon
More info  

.: Specialized Tear Integration for dry eye syndrome in diabetics

There is no doubt that the majority of ophthalmologists and patients indissolubly link diabetes with retinal complications, that is with diabetic retinopathy.
It is known however, that diabetes results in other serious problems of the eye and, taking international literature into consideration, problems of the eye surface linked to this pathology increasingly call for the attention of researchers.
In particular, the biggest worry seems to be the level of damage to the corneal epithelium which can occur during the course of this disease.
This damage to the corneal epithelium seems to relate to a state of general decay of the nervous system linked to hyperglycemia, which, in some cases also involves the sensitive corneal nerve endings (diabetic neuropathy).
The sensitive corneal nerve endings respond to trophic needs and the moisture of the corneal tissue, sending messages to the lachrymal gland and the muciparous cells.
Alteration of this communication system results in lachrymal hyposecretion of increasing intensity, the seriousness of which may not be perceived by the patient, simply because they are affected by diabetic neurodystrophy of the cornea. This can result in serious alteration of this tissue which can manifest itself in what is known internationally as diabetic keratopathy.
When diagnosing this problem in a diabetic, is one faced with simple lachrymal hyposecretion or is it something more?
It is certainly something more, and therefore requires specific treatment with a product which responds adequately to lachrymal hyposecretion with very particular characteristics.
Careful studies on the therapeutic aspects of this disease have led to the development of TIORETIN® eyedrops which is a preparation based on lipoic acid, a molecule with very interesting characteristics.
Indeed, lipoic acid is a powerful antioxidant, participating in the regeneration of antioxidant enzyme complexes of fundamental importance in various tissues, as well as essential vitamins such as vitamins E and C, encouraging cell metabolism (it is an integral part of pyruvate dehydrogenase).
Lipoic acid also has a particular characteristic: it is a small molecule which easily reaches the anatomical areas where it carries out its important biological action.
Thanks to lipoic acid, TIORETIN® eyedrops have the following effects: epithelioprotective, trophic, neuroprotective and neurotrophic.
The aim of TIORETIN® eyedrops is to prevent degeneration of the corneal epithelium, maintain the efficiency of the sensitive corneal nerve endings and maintain adequate production of the lachrymal film.
In TIORETIN® eyedrops, lipoic acid has been associated with hypromellose, a substance with a lubricant and stablizing effect on the lachrymal film as well as having marked mucomimetic qualities, an ideal combination to achieve pre-established objectives: to help the diabetic patient to reduce discomfort tied to alterations in the lachrymal film and avoid the progression of the problem into more serious diseases.
TIORETIN® eyedrops also contain an innovative preservative complex based on N-IG + EDTA. This preservative complex (bactericide and antimicotic) has been shown to be very safe to use in the eye, in so far as it is non-sensitizing, non-irritant and non-epitheliotoxic. TIORETIN® eyedrops are the first eyedrops to be specifically developed for diabetics. The recommended dose is one drop into the conjunctival sac, 3 times a day or more, according to doctor’s instructions.

 
down
down
icon
Download  

News dall'Oftalmologia mondiale

icon_pdf
L'occhio Secco nel paziente diabetico (448 Kb)

Poster N-IG
Efficacia di un nuovo conservante per soluzioni oftalmiche

icon_pdf
Poster N-IG (2,2 Mb)
down
down
icon_biblio
Bibliography

1. Corneal epithelium in diabetic patient . Kenzo Tzuboda, M.D. et al Cornea 10 (2): 156-160,1991.

2. Corneal epithelium barrier function in diabetic patient. Mamomu Gekka, M.D. et al Cornea volume 23, Numero 1, january 2004.

3. Changes in the tear proteins of diabetic patients F H Grus* 1, P Sabuncuo 1, H B Dick1, A J Augustin2 and N Pfeiffer1 BMC Ophthalmology 2002, 2:4.

4. Correlation of corneal sensation , but not of basal or reflex tear secretion, with the stage of diabetic retinopaty. Jun Saito,M . D. et al. Cornea 22(1): 15-18, 2003.

5. Etude des atteintes de la suface oculaire chez les patient diabetiques. C. Creuzot-garcher et al. J.Fr. Opatolmo. 2005; 28, 6, 583-588.

6. Noninvasive Assessment of Corneal Sensitivity in Young and Elderly Diabetic and Nondiabetic Subjects Paul J. Murphy,1 Sudi Patel, 2, 3 Ngai Kong,4 Robert E. J. Ryder, 5 and John Marshall 6 (Invest Ophthalmol Vis Sci. 2004; 45: 1737-1742) DOI: 10.1167/iovs. 03-0689.

7. Tear Function and Ocular Surface Changes in Noninsulin-dependent Diabetes Mellitu Murat Dogru, MD, PhD, Chikako Katakami, MD, PhD, Masanori Inoue, MD, PhD Ophthalmology 2001;108:586–592 © 2001 by the American Academy of Ophthalmology.

8. Br J Ophthalmol. 2000 Jan; 84(1): 19-21. Comment in: Br J Ophthalmol. 2000. Oct; 84(10): 1210. Tear secretion and tear film function in insulin dependent diabetics. Goebbels M.

9. Ocular and systemic factors relevant to diabetic keratoepitheliopathy, Kenji Inoue ,M.D. et al. Cornea 20(8): 798-801,2001.

10. Is there a correlation between the severità of diabetic retinopaty and keratoconjuntivitis sicca? Johannes Nepp, M.D. et al. Cornea 19(4): 187-191, 2000.

11. Podda M, Tritschler HJ, Ulrich H, Packer L. Alpha-lipoic acid supplementation prevents symptoms of vitamin E deficiency. Biochem Biophys Res Commun. 1994 Oct14; 204(1): 98-104.

12. Biewenga GP, Haenen GR, Bast A The pharmacology of the antioxidant lipoic acid. Gen Pharmacol. 1997 Sep; 29(3): 315-31. Review.
13. FERSHT Alan, STRUTTURA E MECCANISMI D'AZIONE DEGLI ENZIMI, Trad. di C. Bongarzoni, revisione di E. Di Mauro, 1989.

14. Hahm JR, Kim BJ, Kim KW. Clinical experience with thioctacid (thioctic acid) in the treatment of distal symmetric polyneuropathy in Korean diabetic patients. J Diabetes Complications. 2004 Mar-Apr; 18(2): 79-85.

15. Ametov AS. et al. The sensory symptoms of diabetic polyneuropathy are improved with alpha-lipoic acid: the SYDNEY trial. Diabetes Care. 2003 Mar; 26(3): 770-6.

16. Androne L, Gavan NA, Veresiu IA, Orasan R. In vivo effect of lipoic acid on lipid peroxidation in patients with diabetic neuropathy. In Vivo. 2000 Mar-Apr; 14(2): 327-30.

17. Handelman GJ, Han D, Tritschler H, Packer L Alpha-lipoic acid reduction by mammalian cells to the dithiol form, and release into the culture medium. Biochem Pharmacol. 1994 May 18; 47(10): 1725-30.

18. Scholich H, Murphy ME, Sies H. Antioxidant activity of dihydrolipoate against microsomal lipid peroxidation and its dependence on alpha-tocopherol. Biochim Biophys Acta. 1989 Feb 20; 1001(3): 256-61.

19. Suzuki YJ, Tsuchiya M, Packer L. Thioctic acid and dihydrolipoic acid are novel antioxidants which interact with reactive oxygen species. Free Radic Res Commun. 1991; 15(5): 255-63

20. Marangon K, Devaraj S, Tirosh O, Packer L, Jialal I Comparison of the effect of alpha-lipoic acid and alpha-tocopherol supplementation on measures of oxidative stress. Free Radic Biol Med. 1999 Nov; 27(9-10): 1114-21.

21. Xu DP, Wells WW alpha-Lipoic acid dependent regeneration of ascorbic acid from dehydroascorbic acid in rat liver mitochondria. J Bioenerg Biomembr. 1996 Feb; 28(1): 77-85

22. M.A. Lemp - R . Marquardt, L’ OCCHIO SECCO, Edizione italiana a cura di D . Spinelli e S. Gambero, Springer

23. Emilia Ghelardi (1), Giulio Luciani (2), Sonia Senesi (1), Mario Campa (1). 1) Dipartimento di Patologia Sperimentale, Biotecnologie Mediche, Infettivologia ed Epidemiologia, Università di Pisa. 2) Direzione Medica SOOFT italia-BIOOS italia. “Efficacia di un nuovo conservante per soluzioni oftalmiche”.

 
down
 
tioretin collirio
Composition

 

Hypromellose 0.3%
Lipoic acid  
N-hydroxymethylglycinate  
Sodium edetate  
 
Description

 

Lipoic acid 0.1%, hypromellose 0.3% ophthalmic solution

It has been definitively ascertained that diabetes causes serious problems to the eyes, not only to the retina but also to other structures in the eye.
Diabetes also causes alterations to the surface of the eye which can lead to damage to the corneal epithelium and the onset of diseases which can compromise quality of life.

These alterations are mainly due to both an imbalance in tear secretion and damage to the cornea innervations.
When the sensitive innervation of the cornea is compromised this results in altered communication between the cornea and the lachrymal glands, with repercussions for their functioning.

The integrity of the corneal nerve pathways is therefore important to guarantee the physiological production of the lachrymal film, whilst damage to these pathways can cause lachrymal hyposecretion of varying degrees. This could be followed by an alteration to the cornea surface and the manifestation of a pathological form known internationally as diabetic keratopathy.

Eye dryness manifests itself in diabetics a few years after the onset of the illness, and therefore, given the often advanced age of patients, may be initially evaluated as classical senile dry eye syndrome which is due, as is well known, to degeneration of the structures involved in the maintenance of the functional physiological equilibrium of the lachrymal film.

Lachrymal hyposecretion in diabetics is different however to other forms of dry eye syndrome and as a result, treatment requires a product which is not a simple tear substitute.

Precise studies of a pathogenetic and clinical nature regarding alterations to the eye surface in diabetics have led to the development of TIORETIN® eyedrops, a preparation based on lipoic acid.
Lipoic acid is a powerful antioxidant which, as has been widely reported in literature, acts to protect and regenerate enzyme complexes of fundamental importance for the cell, such as the enzyme pyruvate dehydrogenase, thus encouraging the improvement or repair of physiological cell metabolism.
Furthermore, it also contributes to the restoration of the biological effects of essential vitamins such as vitamin E and vitamin C.
Because of its pharmacokinetic properties and thanks also to the fact that it is a small molecule, lipoic acid easily reaches the anatomical areas where it has its important biological effect.

TIORETIN® eyedrops, as a result of the properties of lipoic acid, can, as such, have a positive effect as an epithelio-protector and neuroprotector of the cornea. The pre-established aim of TIORETIN® eyedrops is that of:
- helping to prevent the degeneration of the corneal epithelium;
- maintaining the efficiency of the sensitive corneal nerve endings;
- maintaining the physiological production of the lachrymal film.

TIORETIN® eyedrops are also made up of hypromellose, a polymer with a lubricant effect, which is able to stabilize the lachrymal film due to its mucomimetic properties, thus helping to maintain the integrity of the tissues bathed in lachrymal fluid.

TIORETIN® eyedrops is a multi-dose preparation which contains an innovative preservative system which has a bactericide and antimicotic effect (N-IG + EDTA) and has been shown to be non-sensitizing, non-irritant and non-epitheliotoxic for the eye surface.

TIORETIN® are the first eyedrops to be specifically developed for diabetics.

 

 
 
Product Use

INDICATIONS
An ophthalmic solution which stabilizes and restores the lachrymal film in the event of histological corneo-conjunctival alterations caused by unbalance of the oxido-reductive cellular potential and an accumulation of free radicals on the eye surface.
This product is particularly useful for conditions of oxidative stress:
- of a metabolic nature (diabetic pathology linked to age)
- of a physico-chemical nature.

DOSAGE AND ADMINISTRATION
Instill 1-2 drops into the conjunctival sac 2-3 times a day, or more, according to doctor’s instructions.

PACKAGE
8 ml bottle.

 
 
 
flaguk end